{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/BICD2","ko":"https://www.mygenelog.com/ko/api/v1/genes/BICD2"},"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":"BICD2","url":"https://www.mygenelog.com/genes/BICD2","variant_count":25,"variants":[{"risk_tier":"standard","rsid":"rs10992447","trait_name":"Waist-to-hip ratio adjusted for BMI","url":"https://www.mygenelog.com/variants/rs10992447"},{"risk_tier":"standard","rsid":"rs1131691347","trait_name":"Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1131691347"},{"risk_tier":"standard","rsid":"rs1263279945","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs1263279945"},{"risk_tier":"standard","rsid":"rs149049262","trait_name":"Waist-hip index","url":"https://www.mygenelog.com/variants/rs149049262"},{"risk_tier":"sensitive","rsid":"rs1554705485","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1554705485"},{"risk_tier":"standard","rsid":"rs1564061982","trait_name":"Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1564061982"},{"risk_tier":"standard","rsid":"rs1587668077","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs1587668077"},{"risk_tier":"standard","rsid":"rs1587668748","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs1587668748"},{"risk_tier":"standard","rsid":"rs1587668769","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs1587668769"},{"risk_tier":"standard","rsid":"rs1587668798","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1587668798"},{"risk_tier":"standard","rsid":"rs1587668852","trait_name":"Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1587668852"},{"risk_tier":"standard","rsid":"rs1587671674","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1587671674"},{"risk_tier":"standard","rsid":"rs1853488507","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs1853488507"},{"risk_tier":"standard","rsid":"rs189444416","trait_name":"GDF2 protein levels","url":"https://www.mygenelog.com/variants/rs189444416"},{"risk_tier":"standard","rsid":"rs2131499515","trait_name":"Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2131499515"},{"risk_tier":"standard","rsid":"rs2131504104","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs2131504104"},{"risk_tier":"standard","rsid":"rs2490442124","trait_name":"Spinal muscular atrophy with lower extremity predominance","url":"https://www.mygenelog.com/variants/rs2490442124"},{"risk_tier":"standard","rsid":"rs371707778","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs371707778"},{"risk_tier":"standard","rsid":"rs376312313","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs376312313"},{"risk_tier":"standard","rsid":"rs398123028","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs398123028"},{"risk_tier":"standard","rsid":"rs398123030","trait_name":"Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures","url":"https://www.mygenelog.com/variants/rs398123030"},{"risk_tier":"standard","rsid":"rs545718274","trait_name":"OGN protein levels","url":"https://www.mygenelog.com/variants/rs545718274"},{"risk_tier":"sensitive","rsid":"rs797044920","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs797044920"},{"risk_tier":"standard","rsid":"rs797045412","trait_name":"Spinal muscular atrophy, lower extremity-predominant, 2, AD","url":"https://www.mygenelog.com/variants/rs797045412"},{"risk_tier":"standard","rsid":"rs912262","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs912262"}]}