{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/BCS1L","ko":"https://www.mygenelog.com/ko/api/v1/genes/BCS1L"},"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":"BCS1L","url":"https://www.mygenelog.com/genes/BCS1L","variant_count":45,"variants":[{"risk_tier":"sensitive","rsid":"rs1006907254","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs1006907254"},{"risk_tier":"sensitive","rsid":"rs1057516346","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs1057516346"},{"risk_tier":"standard","rsid":"rs1057516802","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs1057516802"},{"risk_tier":"sensitive","rsid":"rs1057516954","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs1057516954"},{"risk_tier":"sensitive","rsid":"rs1057521059","trait_name":"Leigh syndrome","url":"https://www.mygenelog.com/variants/rs1057521059"},{"risk_tier":"standard","rsid":"rs121908571","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs121908571"},{"risk_tier":"standard","rsid":"rs121908572","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs121908572"},{"risk_tier":"standard","rsid":"rs121908573","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs121908573"},{"risk_tier":"standard","rsid":"rs121908575","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs121908575"},{"risk_tier":"standard","rsid":"rs121908576","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs121908576"},{"risk_tier":"sensitive","rsid":"rs121908577","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs121908577"},{"risk_tier":"sensitive","rsid":"rs121908578","trait_name":"BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY","url":"https://www.mygenelog.com/variants/rs121908578"},{"risk_tier":"sensitive","rsid":"rs121908579","trait_name":"BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY","url":"https://www.mygenelog.com/variants/rs121908579"},{"risk_tier":"standard","rsid":"rs121908580","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs121908580"},{"risk_tier":"sensitive","rsid":"rs1280810181","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs1280810181"},{"risk_tier":"sensitive","rsid":"rs1443643776","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs1443643776"},{"risk_tier":"standard","rsid":"rs144885874","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs144885874"},{"risk_tier":"sensitive","rsid":"rs1553596761","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs1553596761"},{"risk_tier":"sensitive","rsid":"rs1559317208","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs1559317208"},{"risk_tier":"sensitive","rsid":"rs1939496203","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs1939496203"},{"risk_tier":"sensitive","rsid":"rs1939594732","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs1939594732"},{"risk_tier":"sensitive","rsid":"rs1939635954","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs1939635954"},{"risk_tier":"sensitive","rsid":"rs201454788","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs201454788"},{"risk_tier":"sensitive","rsid":"rs2106320484","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs2106320484"},{"risk_tier":"sensitive","rsid":"rs2106324466","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs2106324466"},{"risk_tier":"standard","rsid":"rs2469871803","trait_name":"Neonatal encephalopathy","url":"https://www.mygenelog.com/variants/rs2469871803"},{"risk_tier":"sensitive","rsid":"rs2469890771","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs2469890771"},{"risk_tier":"sensitive","rsid":"rs28937590","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs28937590"},{"risk_tier":"standard","rsid":"rs35843327","trait_name":"Physical function (baseline)","url":"https://www.mygenelog.com/variants/rs35843327"},{"risk_tier":"standard","rsid":"rs369691608","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/variants/rs369691608"},{"risk_tier":"sensitive","rsid":"rs373105002","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs373105002"},{"risk_tier":"standard","rsid":"rs377025174","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs377025174"},{"risk_tier":"sensitive","rsid":"rs386833856","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs386833856"},{"risk_tier":"sensitive","rsid":"rs550497120","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs550497120"},{"risk_tier":"sensitive","rsid":"rs587777278","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs587777278"},{"risk_tier":"sensitive","rsid":"rs749196764","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs749196764"},{"risk_tier":"standard","rsid":"rs754291622","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs754291622"},{"risk_tier":"sensitive","rsid":"rs754414954","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs754414954"},{"risk_tier":"sensitive","rsid":"rs754934987","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs754934987"},{"risk_tier":"sensitive","rsid":"rs762980642","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs762980642"},{"risk_tier":"sensitive","rsid":"rs770749420","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs770749420"},{"risk_tier":"sensitive","rsid":"rs774688562","trait_name":"Pili torti-deafness syndrome","url":"https://www.mygenelog.com/variants/rs774688562"},{"risk_tier":"standard","rsid":"rs776838028","trait_name":"Mitochondrial complex III deficiency nuclear type 1","url":"https://www.mygenelog.com/variants/rs776838028"},{"risk_tier":"sensitive","rsid":"rs779331797","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs779331797"},{"risk_tier":"sensitive","rsid":"rs898301590","trait_name":"GRACILE syndrome","url":"https://www.mygenelog.com/variants/rs898301590"}]}