{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SQSTM1","ko":"https://www.mygenelog.com/ko/api/v1/genes/SQSTM1"},"condition_count":2,"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":"SQSTM1","url":"https://www.mygenelog.com/genes/SQSTM1","variant_count":20,"variants":[{"risk_tier":"sensitive","rsid":"rs104893941","trait_name":"Osteitis deformans [Paget's disease of bone] (PheCode 731.1)","url":"https://www.mygenelog.com/variants/rs104893941"},{"risk_tier":"standard","rsid":"rs11742873","trait_name":"Lymphocyte count","url":"https://www.mygenelog.com/variants/rs11742873"},{"risk_tier":"sensitive","rsid":"rs1185406298","trait_name":"Paget disease of bone 2, early-onset","url":"https://www.mygenelog.com/variants/rs1185406298"},{"risk_tier":"sensitive","rsid":"rs1247551175","trait_name":"Frontotemporal dementia and/or amyotrophic lateral sclerosis 1","url":"https://www.mygenelog.com/variants/rs1247551175"},{"risk_tier":"standard","rsid":"rs1304560157","trait_name":"Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","url":"https://www.mygenelog.com/variants/rs1304560157"},{"risk_tier":"sensitive","rsid":"rs1391182750","trait_name":"Paget disease of bone 2, early-onset","url":"https://www.mygenelog.com/variants/rs1391182750"},{"risk_tier":"sensitive","rsid":"rs1425863340","trait_name":"Paget disease of bone 2, early-onset","url":"https://www.mygenelog.com/variants/rs1425863340"},{"risk_tier":"sensitive","rsid":"rs1757759029","trait_name":"Paget disease of bone 2, early-onset","url":"https://www.mygenelog.com/variants/rs1757759029"},{"risk_tier":"sensitive","rsid":"rs1758351897","trait_name":"Paget disease of bone 2, early-onset","url":"https://www.mygenelog.com/variants/rs1758351897"},{"risk_tier":"sensitive","rsid":"rs2113485289","trait_name":"Frontotemporal dementia and/or amyotrophic lateral sclerosis 1","url":"https://www.mygenelog.com/variants/rs2113485289"},{"risk_tier":"standard","rsid":"rs2113485292","trait_name":"Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","url":"https://www.mygenelog.com/variants/rs2113485292"},{"risk_tier":"sensitive","rsid":"rs2113512370","trait_name":"Paget disease of bone 2, early-onset","url":"https://www.mygenelog.com/variants/rs2113512370"},{"risk_tier":"sensitive","rsid":"rs2480244231","trait_name":"Frontotemporal dementia and/or amyotrophic lateral sclerosis 1","url":"https://www.mygenelog.com/variants/rs2480244231"},{"risk_tier":"sensitive","rsid":"rs373306317","trait_name":"Frontotemporal dementia and/or amyotrophic lateral sclerosis 1","url":"https://www.mygenelog.com/variants/rs373306317"},{"risk_tier":"standard","rsid":"rs56998314","trait_name":"Monocyte percentage of white cells","url":"https://www.mygenelog.com/variants/rs56998314"},{"risk_tier":"sensitive","rsid":"rs771966860","trait_name":"Frontotemporal dementia and/or amyotrophic lateral sclerosis 1","url":"https://www.mygenelog.com/variants/rs771966860"},{"risk_tier":"sensitive","rsid":"rs796051870","trait_name":"Paget disease of bone 3","url":"https://www.mygenelog.com/variants/rs796051870"},{"risk_tier":"sensitive","rsid":"rs796052213","trait_name":"Paget disease of bone 3","url":"https://www.mygenelog.com/variants/rs796052213"},{"risk_tier":"standard","rsid":"rs886039780","trait_name":"Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","url":"https://www.mygenelog.com/variants/rs886039780"},{"risk_tier":"standard","rsid":"rs886039782","trait_name":"Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","url":"https://www.mygenelog.com/variants/rs886039782"}]}