{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/COL11A1","ko":"https://www.mygenelog.com/ko/api/v1/genes/COL11A1"},"condition_count":9,"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":"COL11A1","url":"https://www.mygenelog.com/genes/COL11A1","variant_count":60,"variants":[{"risk_tier":"standard","rsid":"rs1064797115","trait_name":"Hearing impairment","url":"https://www.mygenelog.com/variants/rs1064797115"},{"risk_tier":"standard","rsid":"rs115085036","trait_name":"Free Cholesterol to Cholesteryl Esters in Small HDL ratio","url":"https://www.mygenelog.com/variants/rs115085036"},{"risk_tier":"standard","rsid":"rs1162597563","trait_name":"Fibrochondrogenesis 1","url":"https://www.mygenelog.com/variants/rs1162597563"},{"risk_tier":"standard","rsid":"rs12026245","trait_name":"Intelligence (MTAG)","url":"https://www.mygenelog.com/variants/rs12026245"},{"risk_tier":"standard","rsid":"rs12046389","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs12046389"},{"risk_tier":"standard","rsid":"rs12121824","trait_name":"Hip circumference adjusted for BMI","url":"https://www.mygenelog.com/variants/rs12121824"},{"risk_tier":"sensitive","rsid":"rs121912943","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs121912943"},{"risk_tier":"sensitive","rsid":"rs121912944","trait_name":"Marshall/Stickler syndrome","url":"https://www.mygenelog.com/variants/rs121912944"},{"risk_tier":"sensitive","rsid":"rs12406439","trait_name":"Carpal tunnel syndrome","url":"https://www.mygenelog.com/variants/rs12406439"},{"risk_tier":"standard","rsid":"rs12756209","trait_name":"Estimated bone mineral density","url":"https://www.mygenelog.com/variants/rs12756209"},{"risk_tier":"standard","rsid":"rs140602617","trait_name":"AMY2A protein levels","url":"https://www.mygenelog.com/variants/rs140602617"},{"risk_tier":"standard","rsid":"rs1415365","trait_name":"Hip circumference adjusted for BMI","url":"https://www.mygenelog.com/variants/rs1415365"},{"risk_tier":"sensitive","rsid":"rs1553193910","trait_name":"Marshall syndrome","url":"https://www.mygenelog.com/variants/rs1553193910"},{"risk_tier":"standard","rsid":"rs1553196233","trait_name":"Hearing impairment","url":"https://www.mygenelog.com/variants/rs1553196233"},{"risk_tier":"sensitive","rsid":"rs1553223152","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs1553223152"},{"risk_tier":"sensitive","rsid":"rs1553234339","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1553234339"},{"risk_tier":"standard","rsid":"rs1557812993","trait_name":"Fibrochondrogenesis","url":"https://www.mygenelog.com/variants/rs1557812993"},{"risk_tier":"sensitive","rsid":"rs1557877041","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs1557877041"},{"risk_tier":"sensitive","rsid":"rs1570712875","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs1570712875"},{"risk_tier":"sensitive","rsid":"rs1570740272","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs1570740272"},{"risk_tier":"standard","rsid":"rs1570781670","trait_name":"Hearing loss, autosomal dominant 37","url":"https://www.mygenelog.com/variants/rs1570781670"},{"risk_tier":"sensitive","rsid":"rs1662763051","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs1662763051"},{"risk_tier":"sensitive","rsid":"rs1663311706","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs1663311706"},{"risk_tier":"standard","rsid":"rs1667208458","trait_name":"Fibrochondrogenesis 1","url":"https://www.mygenelog.com/variants/rs1667208458"},{"risk_tier":"standard","rsid":"rs186665133","trait_name":"AMY1A or AMY1B or AMY1C protein levels","url":"https://www.mygenelog.com/variants/rs186665133"},{"risk_tier":"sensitive","rsid":"rs2100852410","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs2100852410"},{"risk_tier":"sensitive","rsid":"rs2101282041","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs2101282041"},{"risk_tier":"sensitive","rsid":"rs2101406339","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2101406339"},{"risk_tier":"sensitive","rsid":"rs2101595036","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2101595036"},{"risk_tier":"sensitive","rsid":"rs2101653580","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2101653580"},{"risk_tier":"standard","rsid":"rs2101678782","trait_name":"Autism","url":"https://www.mygenelog.com/variants/rs2101678782"},{"risk_tier":"standard","rsid":"rs2101794024","trait_name":"Hearing loss, autosomal dominant 37","url":"https://www.mygenelog.com/variants/rs2101794024"},{"risk_tier":"sensitive","rsid":"rs2101800665","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2101800665"},{"risk_tier":"sensitive","rsid":"rs2101869722","trait_name":"Stickler syndrome","url":"https://www.mygenelog.com/variants/rs2101869722"},{"risk_tier":"standard","rsid":"rs2376262","trait_name":"Hip circumference adjusted for BMI","url":"https://www.mygenelog.com/variants/rs2376262"},{"risk_tier":"sensitive","rsid":"rs2524255933","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs2524255933"},{"risk_tier":"sensitive","rsid":"rs2524264000","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs2524264000"},{"risk_tier":"sensitive","rsid":"rs2524540006","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2524540006"},{"risk_tier":"sensitive","rsid":"rs2524570658","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs2524570658"},{"risk_tier":"sensitive","rsid":"rs2524688567","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2524688567"},{"risk_tier":"sensitive","rsid":"rs2524792669","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs2524792669"},{"risk_tier":"sensitive","rsid":"rs2525109250","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2525109250"},{"risk_tier":"sensitive","rsid":"rs2525370664","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs2525370664"},{"risk_tier":"standard","rsid":"rs2616003","trait_name":"Hip circumference adjusted for BMI","url":"https://www.mygenelog.com/variants/rs2616003"},{"risk_tier":"standard","rsid":"rs35037054","trait_name":"Height (baseline)","url":"https://www.mygenelog.com/variants/rs35037054"},{"risk_tier":"sensitive","rsid":"rs372419698","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs372419698"},{"risk_tier":"standard","rsid":"rs3767272","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs3767272"},{"risk_tier":"standard","rsid":"rs387906611","trait_name":"Fibrochondrogenesis","url":"https://www.mygenelog.com/variants/rs387906611"},{"risk_tier":"sensitive","rsid":"rs398122828","trait_name":"Marshall syndrome","url":"https://www.mygenelog.com/variants/rs398122828"},{"risk_tier":"sensitive","rsid":"rs4098282","trait_name":"Osteoarthritis","url":"https://www.mygenelog.com/variants/rs4098282"},{"risk_tier":"standard","rsid":"rs4908289","trait_name":"Hip circumference adjusted for BMI","url":"https://www.mygenelog.com/variants/rs4908289"},{"risk_tier":"standard","rsid":"rs587782990","trait_name":"sporadic abdominal aortic aneurysm","url":"https://www.mygenelog.com/variants/rs587782990"},{"risk_tier":"standard","rsid":"rs747787770","trait_name":"Hearing loss, autosomal dominant 37","url":"https://www.mygenelog.com/variants/rs747787770"},{"risk_tier":"sensitive","rsid":"rs749419834","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs749419834"},{"risk_tier":"standard","rsid":"rs755987732","trait_name":"Fibrochondrogenesis 1","url":"https://www.mygenelog.com/variants/rs755987732"},{"risk_tier":"sensitive","rsid":"rs766849561","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs766849561"},{"risk_tier":"sensitive","rsid":"rs776004614","trait_name":"COL11A1-related disorder","url":"https://www.mygenelog.com/variants/rs776004614"},{"risk_tier":"sensitive","rsid":"rs866783525","trait_name":"Stickler syndrome type 2","url":"https://www.mygenelog.com/variants/rs866783525"},{"risk_tier":"standard","rsid":"rs886042653","trait_name":"Hearing loss, autosomal dominant 37","url":"https://www.mygenelog.com/variants/rs886042653"},{"risk_tier":"sensitive","rsid":"rs886044244","trait_name":"Neurodevelopmental disorder","url":"https://www.mygenelog.com/variants/rs886044244"}]}