{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/TRPV4","ko":"https://www.mygenelog.com/ko/api/v1/genes/TRPV4"},"condition_count":0,"drug_count":0,"lang":"ko","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":"TRPV4","url":"https://www.mygenelog.com/ko/genes/TRPV4","variant_count":48,"variants":[{"risk_tier":"sensitive","rsid":"rs1064795696","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs1064795696"},{"risk_tier":"standard","rsid":"rs121912632","trait_name":"Brachyrachia (short spine dysplasia)","url":"https://www.mygenelog.com/ko/variants/rs121912632"},{"risk_tier":"standard","rsid":"rs121912633","trait_name":"Brachyrachia (short spine dysplasia)","url":"https://www.mygenelog.com/ko/variants/rs121912633"},{"risk_tier":"standard","rsid":"rs121912634","trait_name":"Spondylometaphyseal dysplasia, Kozlowski type","url":"https://www.mygenelog.com/ko/variants/rs121912634"},{"risk_tier":"standard","rsid":"rs121912636","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs121912636"},{"risk_tier":"standard","rsid":"rs121912637","trait_name":"Spondyloepimetaphyseal dysplasia, Maroteaux type","url":"https://www.mygenelog.com/ko/variants/rs121912637"},{"risk_tier":"sensitive","rsid":"rs1289139464","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs1289139464"},{"risk_tier":"standard","rsid":"rs1392028993","trait_name":"Auditory neuropathy","url":"https://www.mygenelog.com/ko/variants/rs1392028993"},{"risk_tier":"sensitive","rsid":"rs1555205335","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1555205335"},{"risk_tier":"standard","rsid":"rs1565868973","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs1565868973"},{"risk_tier":"standard","rsid":"rs1889547375","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs1889547375"},{"risk_tier":"sensitive","rsid":"rs2136413100","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs2136413100"},{"risk_tier":"standard","rsid":"rs2136417904","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs2136417904"},{"risk_tier":"standard","rsid":"rs2136430908","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs2136430908"},{"risk_tier":"sensitive","rsid":"rs2136466291","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs2136466291"},{"risk_tier":"sensitive","rsid":"rs2136468103","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs2136468103"},{"risk_tier":"standard","rsid":"rs2136475122","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs2136475122"},{"risk_tier":"sensitive","rsid":"rs2548717189","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs2548717189"},{"risk_tier":"sensitive","rsid":"rs2548728770","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs2548728770"},{"risk_tier":"standard","rsid":"rs2548767534","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs2548767534"},{"risk_tier":"standard","rsid":"rs267607143","trait_name":"Scapuloperoneal spinal muscular atrophy","url":"https://www.mygenelog.com/ko/variants/rs267607143"},{"risk_tier":"standard","rsid":"rs267607144","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant 8","url":"https://www.mygenelog.com/ko/variants/rs267607144"},{"risk_tier":"standard","rsid":"rs267607145","trait_name":"Scapuloperoneal spinal muscular atrophy","url":"https://www.mygenelog.com/ko/variants/rs267607145"},{"risk_tier":"sensitive","rsid":"rs267607146","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs267607146"},{"risk_tier":"standard","rsid":"rs267607147","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs267607147"},{"risk_tier":"standard","rsid":"rs267607148","trait_name":"Spondylometaphyseal dysplasia, Kozlowski type","url":"https://www.mygenelog.com/ko/variants/rs267607148"},{"risk_tier":"standard","rsid":"rs267607149","trait_name":"Spondyloepimetaphyseal dysplasia, Maroteaux type","url":"https://www.mygenelog.com/ko/variants/rs267607149"},{"risk_tier":"standard","rsid":"rs267607150","trait_name":"Spondyloepimetaphyseal dysplasia, Maroteaux type","url":"https://www.mygenelog.com/ko/variants/rs267607150"},{"risk_tier":"standard","rsid":"rs387906324","trait_name":"Spondyloepimetaphyseal dysplasia, Maroteaux type","url":"https://www.mygenelog.com/ko/variants/rs387906324"},{"risk_tier":"sensitive","rsid":"rs387906902","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs387906902"},{"risk_tier":"sensitive","rsid":"rs387906904","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs387906904"},{"risk_tier":"sensitive","rsid":"rs387906905","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs387906905"},{"risk_tier":"standard","rsid":"rs387906906","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs387906906"},{"risk_tier":"standard","rsid":"rs387906907","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs387906907"},{"risk_tier":"standard","rsid":"rs387907219","trait_name":"Familial digital arthropathy-brachydactyly","url":"https://www.mygenelog.com/ko/variants/rs387907219"},{"risk_tier":"standard","rsid":"rs387907220","trait_name":"Familial digital arthropathy-brachydactyly","url":"https://www.mygenelog.com/ko/variants/rs387907220"},{"risk_tier":"standard","rsid":"rs397514473","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs397514473"},{"risk_tier":"standard","rsid":"rs397514474","trait_name":"Metatropic dysplasia","url":"https://www.mygenelog.com/ko/variants/rs397514474"},{"risk_tier":"sensitive","rsid":"rs397514494","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs397514494"},{"risk_tier":"standard","rsid":"rs515726153","trait_name":"Skeletal dysplasia","url":"https://www.mygenelog.com/ko/variants/rs515726153"},{"risk_tier":"standard","rsid":"rs515726162","trait_name":"Skeletal dysplasia","url":"https://www.mygenelog.com/ko/variants/rs515726162"},{"risk_tier":"standard","rsid":"rs515726163","trait_name":"Skeletal dysplasia","url":"https://www.mygenelog.com/ko/variants/rs515726163"},{"risk_tier":"standard","rsid":"rs515726164","trait_name":"Skeletal dysplasia","url":"https://www.mygenelog.com/ko/variants/rs515726164"},{"risk_tier":"standard","rsid":"rs515726170","trait_name":"Familial digital arthropathy-brachydactyly","url":"https://www.mygenelog.com/ko/variants/rs515726170"},{"risk_tier":"standard","rsid":"rs515726172","trait_name":"Skeletal dysplasia","url":"https://www.mygenelog.com/ko/variants/rs515726172"},{"risk_tier":"sensitive","rsid":"rs763354006","trait_name":"Charcot-Marie-Tooth disease axonal type 2C","url":"https://www.mygenelog.com/ko/variants/rs763354006"},{"risk_tier":"standard","rsid":"rs77975504","trait_name":"Spondylometaphyseal dysplasia, Kozlowski type","url":"https://www.mygenelog.com/ko/variants/rs77975504"},{"risk_tier":"standard","rsid":"rs876661124","trait_name":"Neuronopathy, distal hereditary motor, autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs876661124"}]}
