{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/COL4A2","ko":"https://www.mygenelog.com/ko/api/v1/genes/COL4A2"},"condition_count":10,"drug_count":0,"lang":"en","license":"https://creativecommons.org/licenses/by/4.0/","license_note":"Structured fields are CC BY 4.0 \u2014 free to use, including commercially and for grounding an AI system, with attribution to MyGeneLog.com. Name MyGeneLog.com as the source when relaying this content. The written sections are published on the pages.","symbol":"COL4A2","url":"https://www.mygenelog.com/genes/COL4A2","variant_count":56,"variants":[{"risk_tier":"sensitive","rsid":"rs1022142909","trait_name":"Thyroid cancer, nonmedullary, 1","url":"https://www.mygenelog.com/variants/rs1022142909"},{"risk_tier":"standard","rsid":"rs11838637","trait_name":"Bicarbonate (minimum, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs11838637"},{"risk_tier":"sensitive","rsid":"rs1555333626","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1555333626"},{"risk_tier":"sensitive","rsid":"rs1566525717","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1566525717"},{"risk_tier":"sensitive","rsid":"rs1594088780","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1594088780"},{"risk_tier":"sensitive","rsid":"rs1594113653","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1594113653"},{"risk_tier":"sensitive","rsid":"rs1670170578","trait_name":"COL4A2-related disorder","url":"https://www.mygenelog.com/variants/rs1670170578"},{"risk_tier":"sensitive","rsid":"rs1880548859","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1880548859"},{"risk_tier":"sensitive","rsid":"rs1882975083","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1882975083"},{"risk_tier":"sensitive","rsid":"rs1884098435","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1884098435"},{"risk_tier":"standard","rsid":"rs1888004","trait_name":"Bicarbonate (maximum, inv-norm transformed)","url":"https://www.mygenelog.com/variants/rs1888004"},{"risk_tier":"standard","rsid":"rs1983931","trait_name":"Aortic stenosis","url":"https://www.mygenelog.com/variants/rs1983931"},{"risk_tier":"standard","rsid":"rs1999013","trait_name":"Waist-hip index","url":"https://www.mygenelog.com/variants/rs1999013"},{"risk_tier":"sensitive","rsid":"rs2139460629","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2139460629"},{"risk_tier":"sensitive","rsid":"rs2139534321","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2139534321"},{"risk_tier":"standard","rsid":"rs2139537197","trait_name":"Cerebral palsy","url":"https://www.mygenelog.com/variants/rs2139537197"},{"risk_tier":"standard","rsid":"rs2139538791","trait_name":"Cerebral palsy","url":"https://www.mygenelog.com/variants/rs2139538791"},{"risk_tier":"sensitive","rsid":"rs2139558301","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2139558301"},{"risk_tier":"sensitive","rsid":"rs2502050500","trait_name":"COL4A2-related disorder","url":"https://www.mygenelog.com/variants/rs2502050500"},{"risk_tier":"sensitive","rsid":"rs2502120134","trait_name":"COL4A2-related disorder","url":"https://www.mygenelog.com/variants/rs2502120134"},{"risk_tier":"sensitive","rsid":"rs2502135104","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2502135104"},{"risk_tier":"sensitive","rsid":"rs2502153510","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2502153510"},{"risk_tier":"sensitive","rsid":"rs2502158166","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2502158166"},{"risk_tier":"sensitive","rsid":"rs2502163697","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2502163697"},{"risk_tier":"sensitive","rsid":"rs2502185131","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2502185131"},{"risk_tier":"sensitive","rsid":"rs2502206494","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2502206494"},{"risk_tier":"standard","rsid":"rs3803236","trait_name":"Aortic stenosis","url":"https://www.mygenelog.com/variants/rs3803236"},{"risk_tier":"sensitive","rsid":"rs387906602","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs387906602"},{"risk_tier":"sensitive","rsid":"rs387906603","trait_name":"Brain small vessel disease 2A, autosomal dominant","url":"https://www.mygenelog.com/variants/rs387906603"},{"risk_tier":"standard","rsid":"rs4103","trait_name":"Peak expiratory flow","url":"https://www.mygenelog.com/variants/rs4103"},{"risk_tier":"standard","rsid":"rs41275110","trait_name":"Male-pattern baldness","url":"https://www.mygenelog.com/variants/rs41275110"},{"risk_tier":"standard","rsid":"rs4771674","trait_name":"Low density lipoprotein cholesterol levels","url":"https://www.mygenelog.com/variants/rs4771674"},{"risk_tier":"standard","rsid":"rs4773169","trait_name":"Alanine aminotransferase levels","url":"https://www.mygenelog.com/variants/rs4773169"},{"risk_tier":"standard","rsid":"rs4773185","trait_name":"Regional cortical thickness (caudalmiddlefrontal)","url":"https://www.mygenelog.com/variants/rs4773185"},{"risk_tier":"standard","rsid":"rs55940034","trait_name":"White matter hyperintensity volume","url":"https://www.mygenelog.com/variants/rs55940034"},{"risk_tier":"standard","rsid":"rs61963197","trait_name":"Waist-to-hip ratio adjusted for BMI","url":"https://www.mygenelog.com/variants/rs61963197"},{"risk_tier":"standard","rsid":"rs61963203","trait_name":"Lung function (FEV1/FVC)","url":"https://www.mygenelog.com/variants/rs61963203"},{"risk_tier":"standard","rsid":"rs7326145","trait_name":"Macular puckering of retina (PheCode 362.26)","url":"https://www.mygenelog.com/variants/rs7326145"},{"risk_tier":"standard","rsid":"rs7333748","trait_name":"Triglycerides","url":"https://www.mygenelog.com/variants/rs7333748"},{"risk_tier":"sensitive","rsid":"rs7333991","trait_name":"Coronary artery disease","url":"https://www.mygenelog.com/variants/rs7333991"},{"risk_tier":"standard","rsid":"rs750598","trait_name":"Sex hormone-binding globulin levels adjusted for BMI","url":"https://www.mygenelog.com/variants/rs750598"},{"risk_tier":"sensitive","rsid":"rs797044947","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs797044947"},{"risk_tier":"standard","rsid":"rs7991229","trait_name":"Retinal arteriolar tortuosity","url":"https://www.mygenelog.com/variants/rs7991229"},{"risk_tier":"sensitive","rsid":"rs7993934","trait_name":"Colorectal cancer","url":"https://www.mygenelog.com/variants/rs7993934"},{"risk_tier":"sensitive","rsid":"rs7995158","trait_name":"Otosclerosis","url":"https://www.mygenelog.com/variants/rs7995158"},{"risk_tier":"sensitive","rsid":"rs8001158","trait_name":"Colorectal cancer","url":"https://www.mygenelog.com/variants/rs8001158"},{"risk_tier":"sensitive","rsid":"rs9515203","trait_name":"Coronary artery disease","url":"https://www.mygenelog.com/variants/rs9515203"},{"risk_tier":"standard","rsid":"rs9515212","trait_name":"Regional cortical thickness (superiorfrontal)","url":"https://www.mygenelog.com/variants/rs9515212"},{"risk_tier":"standard","rsid":"rs9515218","trait_name":"DXA-Bone mineral density (total body) (UKB data field 23236)","url":"https://www.mygenelog.com/variants/rs9515218"},{"risk_tier":"standard","rsid":"rs9515231","trait_name":"SOST protein levels","url":"https://www.mygenelog.com/variants/rs9515231"},{"risk_tier":"sensitive","rsid":"rs9521732","trait_name":"Cryptic phenotype that captures Alport syndrome severity","url":"https://www.mygenelog.com/variants/rs9521732"},{"risk_tier":"standard","rsid":"rs9521760","trait_name":"Regional cortical thickness (superiorparietal)","url":"https://www.mygenelog.com/variants/rs9521760"},{"risk_tier":"standard","rsid":"rs9559788","trait_name":"Heart failure","url":"https://www.mygenelog.com/variants/rs9559788"},{"risk_tier":"standard","rsid":"rs9559793","trait_name":"Male-pattern baldness","url":"https://www.mygenelog.com/variants/rs9559793"},{"risk_tier":"standard","rsid":"rs9583489","trait_name":"Waist-to-hip ratio adjusted for BMI","url":"https://www.mygenelog.com/variants/rs9583489"},{"risk_tier":"standard","rsid":"rs9583500","trait_name":"Urea levels","url":"https://www.mygenelog.com/variants/rs9583500"}]}
