{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/CHD7","ko":"https://www.mygenelog.com/ko/api/v1/genes/CHD7"},"condition_count":8,"drug_count":0,"lang":"en","license":"https://creativecommons.org/licenses/by-nc/4.0/","license_note":"This response is CC BY-NC 4.0 \u2014 free for non-commercial use with attribution to MyGeneLog.com. Name MyGeneLog.com as the source and give the page URL when relaying this content. Commercial use (a product you sell or operate, internal use inside a company, training or serving a commercial AI system) needs a licence: API Pro covers internal use, API Business covers a product, and a content and data licence covers everything else \u2014 https://www.mygenelog.com/license. Facts themselves (an rsID, a ClinVar classification, a p-value) are not copyrightable and are not what the licence covers; the wording, the Korean, the assembly and the graph are.","symbol":"CHD7","url":"https://www.mygenelog.com/genes/CHD7","variant_count":256,"variants":[{"risk_tier":"sensitive","rsid":"rs1021645395","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1021645395"},{"risk_tier":"sensitive","rsid":"rs1024600310","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1024600310"},{"risk_tier":"sensitive","rsid":"rs1057517956","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1057517956"},{"risk_tier":"sensitive","rsid":"rs1057519423","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1057519423"},{"risk_tier":"sensitive","rsid":"rs1057521077","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1057521077"},{"risk_tier":"sensitive","rsid":"rs1057521078","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1057521078"},{"risk_tier":"sensitive","rsid":"rs1060503180","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1060503180"},{"risk_tier":"sensitive","rsid":"rs1060503182","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1060503182"},{"risk_tier":"sensitive","rsid":"rs1060503183","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1060503183"},{"risk_tier":"sensitive","rsid":"rs1060503187","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1060503187"},{"risk_tier":"sensitive","rsid":"rs1060503188","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1060503188"},{"risk_tier":"sensitive","rsid":"rs1064793346","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1064793346"},{"risk_tier":"sensitive","rsid":"rs1064793994","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs1064793994"},{"risk_tier":"sensitive","rsid":"rs1064794250","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1064794250"},{"risk_tier":"sensitive","rsid":"rs1085307582","trait_name":"Thyroid cancer, nonmedullary, 1","url":"https://www.mygenelog.com/variants/rs1085307582"},{"risk_tier":"sensitive","rsid":"rs1131692325","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1131692325"},{"risk_tier":"sensitive","rsid":"rs121434338","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434338"},{"risk_tier":"sensitive","rsid":"rs121434339","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434339"},{"risk_tier":"sensitive","rsid":"rs121434340","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434340"},{"risk_tier":"sensitive","rsid":"rs121434341","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434341"},{"risk_tier":"sensitive","rsid":"rs121434342","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434342"},{"risk_tier":"sensitive","rsid":"rs121434343","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434343"},{"risk_tier":"sensitive","rsid":"rs121434344","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs121434344"},{"risk_tier":"sensitive","rsid":"rs1220292735","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1220292735"},{"risk_tier":"sensitive","rsid":"rs1320897198","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1320897198"},{"risk_tier":"standard","rsid":"rs13256023","trait_name":"Bone marrow fat fraction of lumbar vertebra 5","url":"https://www.mygenelog.com/variants/rs13256023"},{"risk_tier":"sensitive","rsid":"rs1341064149","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1341064149"},{"risk_tier":"sensitive","rsid":"rs1360515765","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1360515765"},{"risk_tier":"sensitive","rsid":"rs1404353688","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1404353688"},{"risk_tier":"standard","rsid":"rs140727637","trait_name":"Eosinophil count","url":"https://www.mygenelog.com/variants/rs140727637"},{"risk_tier":"sensitive","rsid":"rs1487550618","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1487550618"},{"risk_tier":"sensitive","rsid":"rs1554581277","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554581277"},{"risk_tier":"sensitive","rsid":"rs1554581399","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554581399"},{"risk_tier":"sensitive","rsid":"rs1554581657","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554581657"},{"risk_tier":"sensitive","rsid":"rs1554593049","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554593049"},{"risk_tier":"sensitive","rsid":"rs1554597465","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554597465"},{"risk_tier":"sensitive","rsid":"rs1554597716","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554597716"},{"risk_tier":"sensitive","rsid":"rs1554598013","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554598013"},{"risk_tier":"sensitive","rsid":"rs1554598029","trait_name":"Hepatocellular carcinoma","url":"https://www.mygenelog.com/variants/rs1554598029"},{"risk_tier":"sensitive","rsid":"rs1554599035","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554599035"},{"risk_tier":"sensitive","rsid":"rs1554599065","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554599065"},{"risk_tier":"sensitive","rsid":"rs1554600633","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs1554600633"},{"risk_tier":"sensitive","rsid":"rs1554602465","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1554602465"},{"risk_tier":"sensitive","rsid":"rs1554602466","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554602466"},{"risk_tier":"sensitive","rsid":"rs1554602587","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554602587"},{"risk_tier":"sensitive","rsid":"rs1554602588","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554602588"},{"risk_tier":"sensitive","rsid":"rs1554603151","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554603151"},{"risk_tier":"sensitive","rsid":"rs1554603276","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554603276"},{"risk_tier":"sensitive","rsid":"rs1554603293","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554603293"},{"risk_tier":"sensitive","rsid":"rs1554603552","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554603552"},{"risk_tier":"sensitive","rsid":"rs1554603589","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1554603589"},{"risk_tier":"sensitive","rsid":"rs1554603672","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554603672"},{"risk_tier":"standard","rsid":"rs1554603970","trait_name":"Hypogonadotropic hypogonadism 5 with or without anosmia","url":"https://www.mygenelog.com/variants/rs1554603970"},{"risk_tier":"sensitive","rsid":"rs1554604915","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554604915"},{"risk_tier":"sensitive","rsid":"rs1554605973","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554605973"},{"risk_tier":"sensitive","rsid":"rs1554606033","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554606033"},{"risk_tier":"sensitive","rsid":"rs1554606274","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1554606274"},{"risk_tier":"sensitive","rsid":"rs1563559596","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563559596"},{"risk_tier":"sensitive","rsid":"rs1563560018","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563560018"},{"risk_tier":"sensitive","rsid":"rs1563560149","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563560149"},{"risk_tier":"sensitive","rsid":"rs1563625351","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563625351"},{"risk_tier":"sensitive","rsid":"rs1563636399","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563636399"},{"risk_tier":"sensitive","rsid":"rs1563643394","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563643394"},{"risk_tier":"sensitive","rsid":"rs1563644066","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563644066"},{"risk_tier":"sensitive","rsid":"rs1563669203","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563669203"},{"risk_tier":"sensitive","rsid":"rs1563669432","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563669432"},{"risk_tier":"sensitive","rsid":"rs1563670964","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1563670964"},{"risk_tier":"sensitive","rsid":"rs1586249808","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586249808"},{"risk_tier":"sensitive","rsid":"rs1586251038","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586251038"},{"risk_tier":"sensitive","rsid":"rs1586350727","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586350727"},{"risk_tier":"sensitive","rsid":"rs1586389929","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586389929"},{"risk_tier":"sensitive","rsid":"rs1586393514","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586393514"},{"risk_tier":"sensitive","rsid":"rs1586393556","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586393556"},{"risk_tier":"sensitive","rsid":"rs1586418093","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586418093"},{"risk_tier":"sensitive","rsid":"rs1586420419","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586420419"},{"risk_tier":"sensitive","rsid":"rs1586437186","trait_name":"Wiedemann-Steiner syndrome","url":"https://www.mygenelog.com/variants/rs1586437186"},{"risk_tier":"sensitive","rsid":"rs1586440484","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586440484"},{"risk_tier":"sensitive","rsid":"rs1586446578","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586446578"},{"risk_tier":"sensitive","rsid":"rs1586451506","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586451506"},{"risk_tier":"sensitive","rsid":"rs1586460329","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586460329"},{"risk_tier":"sensitive","rsid":"rs1586466948","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1586466948"},{"risk_tier":"sensitive","rsid":"rs1804054410","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804054410"},{"risk_tier":"standard","rsid":"rs1804098617","trait_name":"Chromatinopathy","url":"https://www.mygenelog.com/variants/rs1804098617"},{"risk_tier":"sensitive","rsid":"rs1804103264","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804103264"},{"risk_tier":"sensitive","rsid":"rs1804153455","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804153455"},{"risk_tier":"sensitive","rsid":"rs1804369859","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804369859"},{"risk_tier":"sensitive","rsid":"rs1804454889","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804454889"},{"risk_tier":"sensitive","rsid":"rs1804800800","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804800800"},{"risk_tier":"sensitive","rsid":"rs1804804514","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804804514"},{"risk_tier":"sensitive","rsid":"rs1804990594","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804990594"},{"risk_tier":"sensitive","rsid":"rs1804993220","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1804993220"},{"risk_tier":"standard","rsid":"rs1805143456","trait_name":"Scoliosis, isolated, susceptibility to, 3","url":"https://www.mygenelog.com/variants/rs1805143456"},{"risk_tier":"sensitive","rsid":"rs1805157634","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805157634"},{"risk_tier":"sensitive","rsid":"rs1805310365","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805310365"},{"risk_tier":"sensitive","rsid":"rs1805338299","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805338299"},{"risk_tier":"sensitive","rsid":"rs1805486327","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805486327"},{"risk_tier":"sensitive","rsid":"rs1805504949","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805504949"},{"risk_tier":"sensitive","rsid":"rs1805513214","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805513214"},{"risk_tier":"sensitive","rsid":"rs1805529214","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805529214"},{"risk_tier":"sensitive","rsid":"rs1805573066","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1805573066"},{"risk_tier":"sensitive","rsid":"rs1806173195","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1806173195"},{"risk_tier":"standard","rsid":"rs1809000474","trait_name":"Hypogonadotropic hypogonadism 5 with or without anosmia","url":"https://www.mygenelog.com/variants/rs1809000474"},{"risk_tier":"sensitive","rsid":"rs1809042353","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1809042353"},{"risk_tier":"sensitive","rsid":"rs1809058275","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1809058275"},{"risk_tier":"sensitive","rsid":"rs1809060881","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1809060881"},{"risk_tier":"sensitive","rsid":"rs1809062715","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1809062715"},{"risk_tier":"sensitive","rsid":"rs1811957737","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs1811957737"},{"risk_tier":"sensitive","rsid":"rs199981784","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs199981784"},{"risk_tier":"sensitive","rsid":"rs200024753","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs200024753"},{"risk_tier":"sensitive","rsid":"rs200220845","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs200220845"},{"risk_tier":"sensitive","rsid":"rs2129644242","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2129644242"},{"risk_tier":"sensitive","rsid":"rs2129644267","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2129644267"},{"risk_tier":"sensitive","rsid":"rs2150577671","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150577671"},{"risk_tier":"sensitive","rsid":"rs2150578792","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150578792"},{"risk_tier":"sensitive","rsid":"rs2150579361","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150579361"},{"risk_tier":"sensitive","rsid":"rs2150580244","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150580244"},{"risk_tier":"sensitive","rsid":"rs2150580758","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150580758"},{"risk_tier":"sensitive","rsid":"rs2150697457","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150697457"},{"risk_tier":"sensitive","rsid":"rs2150711063","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150711063"},{"risk_tier":"sensitive","rsid":"rs2150739058","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150739058"},{"risk_tier":"sensitive","rsid":"rs2150749475","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150749475"},{"risk_tier":"sensitive","rsid":"rs2150750132","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150750132"},{"risk_tier":"sensitive","rsid":"rs2150764574","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150764574"},{"risk_tier":"sensitive","rsid":"rs2150779252","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150779252"},{"risk_tier":"sensitive","rsid":"rs2150779267","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150779267"},{"risk_tier":"sensitive","rsid":"rs2150793053","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150793053"},{"risk_tier":"sensitive","rsid":"rs2150794309","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150794309"},{"risk_tier":"sensitive","rsid":"rs2150808631","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150808631"},{"risk_tier":"sensitive","rsid":"rs2150808654","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150808654"},{"risk_tier":"sensitive","rsid":"rs2150809777","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2150809777"},{"risk_tier":"standard","rsid":"rs2272727","trait_name":"Smoking initiation","url":"https://www.mygenelog.com/variants/rs2272727"},{"risk_tier":"sensitive","rsid":"rs2487257832","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487257832"},{"risk_tier":"sensitive","rsid":"rs2487263004","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487263004"},{"risk_tier":"sensitive","rsid":"rs2487264136","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487264136"},{"risk_tier":"sensitive","rsid":"rs2487264288","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487264288"},{"risk_tier":"sensitive","rsid":"rs2487267049","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487267049"},{"risk_tier":"sensitive","rsid":"rs2487283883","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487283883"},{"risk_tier":"sensitive","rsid":"rs2487285824","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487285824"},{"risk_tier":"sensitive","rsid":"rs2487541533","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs2487541533"},{"risk_tier":"sensitive","rsid":"rs2487681882","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487681882"},{"risk_tier":"sensitive","rsid":"rs2487804678","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487804678"},{"risk_tier":"sensitive","rsid":"rs2487805950","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487805950"},{"risk_tier":"sensitive","rsid":"rs2487807451","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487807451"},{"risk_tier":"sensitive","rsid":"rs2487807791","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487807791"},{"risk_tier":"sensitive","rsid":"rs2487807806","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487807806"},{"risk_tier":"sensitive","rsid":"rs2487811001","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2487811001"},{"risk_tier":"sensitive","rsid":"rs2487819601","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487819601"},{"risk_tier":"sensitive","rsid":"rs2487852842","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487852842"},{"risk_tier":"sensitive","rsid":"rs2487853842","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487853842"},{"risk_tier":"sensitive","rsid":"rs2487894669","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2487894669"},{"risk_tier":"sensitive","rsid":"rs2487895579","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487895579"},{"risk_tier":"sensitive","rsid":"rs2487896744","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487896744"},{"risk_tier":"sensitive","rsid":"rs2487897230","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487897230"},{"risk_tier":"sensitive","rsid":"rs2487902725","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs2487902725"},{"risk_tier":"sensitive","rsid":"rs2487902736","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487902736"},{"risk_tier":"sensitive","rsid":"rs2487910301","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs2487910301"},{"risk_tier":"sensitive","rsid":"rs2487910556","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487910556"},{"risk_tier":"sensitive","rsid":"rs2487911129","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2487911129"},{"risk_tier":"sensitive","rsid":"rs2487913969","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487913969"},{"risk_tier":"sensitive","rsid":"rs2487944279","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2487944279"},{"risk_tier":"sensitive","rsid":"rs2487945576","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2487945576"},{"risk_tier":"sensitive","rsid":"rs2487948749","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487948749"},{"risk_tier":"sensitive","rsid":"rs2487976398","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487976398"},{"risk_tier":"sensitive","rsid":"rs2487998998","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2487998998"},{"risk_tier":"sensitive","rsid":"rs2488004616","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488004616"},{"risk_tier":"sensitive","rsid":"rs2488023566","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488023566"},{"risk_tier":"sensitive","rsid":"rs2488024296","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs2488024296"},{"risk_tier":"sensitive","rsid":"rs2488029385","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488029385"},{"risk_tier":"sensitive","rsid":"rs2488030349","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488030349"},{"risk_tier":"sensitive","rsid":"rs2488032118","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488032118"},{"risk_tier":"sensitive","rsid":"rs2488035178","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488035178"},{"risk_tier":"sensitive","rsid":"rs2488037309","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs2488037309"},{"risk_tier":"sensitive","rsid":"rs2488041508","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488041508"},{"risk_tier":"sensitive","rsid":"rs2488042663","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488042663"},{"risk_tier":"sensitive","rsid":"rs2488056320","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488056320"},{"risk_tier":"sensitive","rsid":"rs2488058064","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488058064"},{"risk_tier":"sensitive","rsid":"rs2488074192","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs2488074192"},{"risk_tier":"sensitive","rsid":"rs2488074863","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs2488074863"},{"risk_tier":"sensitive","rsid":"rs267606724","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs267606724"},{"risk_tier":"standard","rsid":"rs35914442","trait_name":"Eosinophil percentage of white cells","url":"https://www.mygenelog.com/variants/rs35914442"},{"risk_tier":"sensitive","rsid":"rs372174845","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs372174845"},{"risk_tier":"sensitive","rsid":"rs376056567","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs376056567"},{"risk_tier":"standard","rsid":"rs3763591","trait_name":"Lymphocytic thyroiditis","url":"https://www.mygenelog.com/variants/rs3763591"},{"risk_tier":"sensitive","rsid":"rs387906271","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs387906271"},{"risk_tier":"sensitive","rsid":"rs398124321","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs398124321"},{"risk_tier":"standard","rsid":"rs4738817","trait_name":"Urinary albumin excretion (no hypertensive medication)","url":"https://www.mygenelog.com/variants/rs4738817"},{"risk_tier":"sensitive","rsid":"rs554737227","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs554737227"},{"risk_tier":"sensitive","rsid":"rs587783428","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783428"},{"risk_tier":"sensitive","rsid":"rs587783429","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783429"},{"risk_tier":"sensitive","rsid":"rs587783432","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783432"},{"risk_tier":"sensitive","rsid":"rs587783433","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783433"},{"risk_tier":"sensitive","rsid":"rs587783434","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783434"},{"risk_tier":"sensitive","rsid":"rs587783440","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783440"},{"risk_tier":"sensitive","rsid":"rs587783441","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783441"},{"risk_tier":"sensitive","rsid":"rs587783442","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783442"},{"risk_tier":"sensitive","rsid":"rs587783445","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783445"},{"risk_tier":"sensitive","rsid":"rs587783446","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783446"},{"risk_tier":"sensitive","rsid":"rs587783447","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783447"},{"risk_tier":"sensitive","rsid":"rs587783448","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783448"},{"risk_tier":"sensitive","rsid":"rs587783450","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783450"},{"risk_tier":"sensitive","rsid":"rs587783451","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783451"},{"risk_tier":"sensitive","rsid":"rs587783454","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783454"},{"risk_tier":"sensitive","rsid":"rs587783455","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783455"},{"risk_tier":"sensitive","rsid":"rs587783457","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783457"},{"risk_tier":"sensitive","rsid":"rs587783458","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783458"},{"risk_tier":"sensitive","rsid":"rs587783459","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs587783459"},{"risk_tier":"standard","rsid":"rs59614411","trait_name":"Retinal thickness (functional principal component 2)","url":"https://www.mygenelog.com/variants/rs59614411"},{"risk_tier":"standard","rsid":"rs60146492","trait_name":"Cortical thickness","url":"https://www.mygenelog.com/variants/rs60146492"},{"risk_tier":"standard","rsid":"rs61675430","trait_name":"Photoreceptor cell layer thickness phenotypes (MTAG)","url":"https://www.mygenelog.com/variants/rs61675430"},{"risk_tier":"standard","rsid":"rs6984890","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs6984890"},{"risk_tier":"standard","rsid":"rs6988835","trait_name":"Mitochondrial DNA copy number (raw)","url":"https://www.mygenelog.com/variants/rs6988835"},{"risk_tier":"sensitive","rsid":"rs727503860","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs727503860"},{"risk_tier":"sensitive","rsid":"rs727503861","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs727503861"},{"risk_tier":"sensitive","rsid":"rs748126701","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs748126701"},{"risk_tier":"sensitive","rsid":"rs748504264","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs748504264"},{"risk_tier":"sensitive","rsid":"rs751709941","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs751709941"},{"risk_tier":"sensitive","rsid":"rs755066542","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs755066542"},{"risk_tier":"sensitive","rsid":"rs757160222","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs757160222"},{"risk_tier":"standard","rsid":"rs75756215","trait_name":"Insomnia","url":"https://www.mygenelog.com/variants/rs75756215"},{"risk_tier":"sensitive","rsid":"rs761214775","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs761214775"},{"risk_tier":"sensitive","rsid":"rs766110936","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs766110936"},{"risk_tier":"sensitive","rsid":"rs766862122","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs766862122"},{"risk_tier":"sensitive","rsid":"rs768152792","trait_name":"CHD7-related disorder","url":"https://www.mygenelog.com/variants/rs768152792"},{"risk_tier":"sensitive","rsid":"rs770166812","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs770166812"},{"risk_tier":"sensitive","rsid":"rs773047607","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs773047607"},{"risk_tier":"sensitive","rsid":"rs773138428","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs773138428"},{"risk_tier":"sensitive","rsid":"rs774255090","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs774255090"},{"risk_tier":"standard","rsid":"rs77753524","trait_name":"Weight","url":"https://www.mygenelog.com/variants/rs77753524"},{"risk_tier":"sensitive","rsid":"rs777652245","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs777652245"},{"risk_tier":"sensitive","rsid":"rs780953224","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs780953224"},{"risk_tier":"standard","rsid":"rs7823926","trait_name":"Smoking initiation","url":"https://www.mygenelog.com/variants/rs7823926"},{"risk_tier":"sensitive","rsid":"rs794727293","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs794727293"},{"risk_tier":"sensitive","rsid":"rs794727423","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs794727423"},{"risk_tier":"sensitive","rsid":"rs794727569","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs794727569"},{"risk_tier":"sensitive","rsid":"rs797045467","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs797045467"},{"risk_tier":"sensitive","rsid":"rs864309609","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs864309609"},{"risk_tier":"sensitive","rsid":"rs864622523","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs864622523"},{"risk_tier":"sensitive","rsid":"rs875989879","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs875989879"},{"risk_tier":"sensitive","rsid":"rs878855031","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs878855031"},{"risk_tier":"sensitive","rsid":"rs878855032","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs878855032"},{"risk_tier":"sensitive","rsid":"rs878975068","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs878975068"},{"risk_tier":"sensitive","rsid":"rs886039526","trait_name":"CHD7-related CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886039526"},{"risk_tier":"standard","rsid":"rs886039881","trait_name":"Hypogonadotropic hypogonadism 5 with or without anosmia","url":"https://www.mygenelog.com/variants/rs886039881"},{"risk_tier":"sensitive","rsid":"rs886040978","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040978"},{"risk_tier":"sensitive","rsid":"rs886040981","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040981"},{"risk_tier":"sensitive","rsid":"rs886040983","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040983"},{"risk_tier":"sensitive","rsid":"rs886040985","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040985"},{"risk_tier":"sensitive","rsid":"rs886040986","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040986"},{"risk_tier":"sensitive","rsid":"rs886040988","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040988"},{"risk_tier":"sensitive","rsid":"rs886040991","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040991"},{"risk_tier":"sensitive","rsid":"rs886040995","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040995"},{"risk_tier":"sensitive","rsid":"rs886040996","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886040996"},{"risk_tier":"sensitive","rsid":"rs886041166","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs886041166"},{"risk_tier":"sensitive","rsid":"rs886041167","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs886041167"},{"risk_tier":"standard","rsid":"rs9298041","trait_name":"Smoking initiation","url":"https://www.mygenelog.com/variants/rs9298041"},{"risk_tier":"sensitive","rsid":"rs985812567","trait_name":"CHARGE syndrome","url":"https://www.mygenelog.com/variants/rs985812567"}]}
