{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SMCHD1","ko":"https://www.mygenelog.com/ko/api/v1/genes/SMCHD1"},"condition_count":5,"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":"SMCHD1","url":"https://www.mygenelog.com/genes/SMCHD1","variant_count":46,"variants":[{"risk_tier":"sensitive","rsid":"rs1057519640","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1057519640"},{"risk_tier":"sensitive","rsid":"rs1057519641","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1057519641"},{"risk_tier":"sensitive","rsid":"rs1057519642","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1057519642"},{"risk_tier":"sensitive","rsid":"rs1057519644","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1057519644"},{"risk_tier":"sensitive","rsid":"rs1057519645","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1057519645"},{"risk_tier":"sensitive","rsid":"rs1057519646","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1057519646"},{"risk_tier":"sensitive","rsid":"rs1135402739","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1135402739"},{"risk_tier":"sensitive","rsid":"rs1135402741","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1135402741"},{"risk_tier":"sensitive","rsid":"rs1135402742","trait_name":"Arrhinia with choanal atresia and microphthalmia syndrome","url":"https://www.mygenelog.com/variants/rs1135402742"},{"risk_tier":"standard","rsid":"rs1224850132","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs1224850132"},{"risk_tier":"standard","rsid":"rs1245372794","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs1245372794"},{"risk_tier":"sensitive","rsid":"rs1248130436","trait_name":"SMCHD1-related disorder","url":"https://www.mygenelog.com/variants/rs1248130436"},{"risk_tier":"standard","rsid":"rs1345926097","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs1345926097"},{"risk_tier":"sensitive","rsid":"rs1555625396","trait_name":"Ch\u00e9diak-Higashi syndrome","url":"https://www.mygenelog.com/variants/rs1555625396"},{"risk_tier":"standard","rsid":"rs1555644339","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs1555644339"},{"risk_tier":"standard","rsid":"rs1598416221","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs1598416221"},{"risk_tier":"standard","rsid":"rs17552342","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs17552342"},{"risk_tier":"standard","rsid":"rs201632358","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs201632358"},{"risk_tier":"standard","rsid":"rs2073049380","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2073049380"},{"risk_tier":"standard","rsid":"rs2075308386","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2075308386"},{"risk_tier":"standard","rsid":"rs2111679","trait_name":"Height (standard GWA)","url":"https://www.mygenelog.com/variants/rs2111679"},{"risk_tier":"standard","rsid":"rs2143182200","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2143182200"},{"risk_tier":"standard","rsid":"rs2143184995","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2143184995"},{"risk_tier":"standard","rsid":"rs2143214372","trait_name":"Abnormality of the musculature","url":"https://www.mygenelog.com/variants/rs2143214372"},{"risk_tier":"standard","rsid":"rs2143367390","trait_name":"Abnormality of the musculature","url":"https://www.mygenelog.com/variants/rs2143367390"},{"risk_tier":"standard","rsid":"rs2143438994","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2143438994"},{"risk_tier":"standard","rsid":"rs2143530610","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2143530610"},{"risk_tier":"standard","rsid":"rs2143805963","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2143805963"},{"risk_tier":"standard","rsid":"rs2347808","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs2347808"},{"risk_tier":"standard","rsid":"rs2510028167","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2510028167"},{"risk_tier":"standard","rsid":"rs2510085323","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2510085323"},{"risk_tier":"standard","rsid":"rs2510097246","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2510097246"},{"risk_tier":"standard","rsid":"rs2510110251","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2510110251"},{"risk_tier":"standard","rsid":"rs2510122804","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs2510122804"},{"risk_tier":"standard","rsid":"rs300295","trait_name":"Body mass index","url":"https://www.mygenelog.com/variants/rs300295"},{"risk_tier":"standard","rsid":"rs377471712","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs377471712"},{"risk_tier":"standard","rsid":"rs397514623","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs397514623"},{"risk_tier":"standard","rsid":"rs474000","trait_name":"Educational attainment","url":"https://www.mygenelog.com/variants/rs474000"},{"risk_tier":"standard","rsid":"rs57126421","trait_name":"Weight","url":"https://www.mygenelog.com/variants/rs57126421"},{"risk_tier":"standard","rsid":"rs685958","trait_name":"Highest math class taken (MTAG)","url":"https://www.mygenelog.com/variants/rs685958"},{"risk_tier":"standard","rsid":"rs7245003","trait_name":"Trunk fat mass (UKB data field 23128)","url":"https://www.mygenelog.com/variants/rs7245003"},{"risk_tier":"standard","rsid":"rs867694014","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs867694014"},{"risk_tier":"standard","rsid":"rs886041918","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs886041918"},{"risk_tier":"standard","rsid":"rs886042417","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs886042417"},{"risk_tier":"standard","rsid":"rs886044369","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs886044369"},{"risk_tier":"standard","rsid":"rs924153704","trait_name":"Facioscapulohumeral muscular dystrophy 2","url":"https://www.mygenelog.com/variants/rs924153704"}]}
