{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/WHRN","ko":"https://www.mygenelog.com/ko/api/v1/genes/WHRN"},"condition_count":3,"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":"WHRN","url":"https://www.mygenelog.com/ko/genes/WHRN","variant_count":17,"variants":[{"risk_tier":"standard","rsid":"rs1075559","trait_name":"Weight","url":"https://www.mygenelog.com/ko/variants/rs1075559"},{"risk_tier":"standard","rsid":"rs137852839","trait_name":"Autosomal recessive nonsyndromic hearing loss 31","url":"https://www.mygenelog.com/ko/variants/rs137852839"},{"risk_tier":"sensitive","rsid":"rs137852840","trait_name":"Usher syndrome type 2D","url":"https://www.mygenelog.com/ko/variants/rs137852840"},{"risk_tier":"standard","rsid":"rs188314624","trait_name":"Hypotony of eye (PheCode 360.3)","url":"https://www.mygenelog.com/ko/variants/rs188314624"},{"risk_tier":"standard","rsid":"rs191980226","trait_name":"ORM1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs191980226"},{"risk_tier":"standard","rsid":"rs193288723","trait_name":"Nonspecific abnormal findings on radiological and other examination of skull and head (PheCode 346.1)","url":"https://www.mygenelog.com/ko/variants/rs193288723"},{"risk_tier":"sensitive","rsid":"rs2133130286","trait_name":"Usher syndrome type 2D","url":"https://www.mygenelog.com/ko/variants/rs2133130286"},{"risk_tier":"sensitive","rsid":"rs2491523011","trait_name":"Usher syndrome type 2D","url":"https://www.mygenelog.com/ko/variants/rs2491523011"},{"risk_tier":"standard","rsid":"rs372472927","trait_name":"Autosomal recessive nonsyndromic hearing loss 31","url":"https://www.mygenelog.com/ko/variants/rs372472927"},{"risk_tier":"standard","rsid":"rs397517255","trait_name":"Rare genetic deafness","url":"https://www.mygenelog.com/ko/variants/rs397517255"},{"risk_tier":"standard","rsid":"rs41278663","trait_name":"ORM1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs41278663"},{"risk_tier":"standard","rsid":"rs533456288","trait_name":"Glycosphingolipids (d42:2) levels","url":"https://www.mygenelog.com/ko/variants/rs533456288"},{"risk_tier":"standard","rsid":"rs543685197","trait_name":"Glycosphingolipids (d42:1) levels","url":"https://www.mygenelog.com/ko/variants/rs543685197"},{"risk_tier":"standard","rsid":"rs74551598","trait_name":"Total cholesterol levels","url":"https://www.mygenelog.com/ko/variants/rs74551598"},{"risk_tier":"standard","rsid":"rs776268964","trait_name":"Autosomal recessive nonsyndromic hearing loss 31","url":"https://www.mygenelog.com/ko/variants/rs776268964"},{"risk_tier":"standard","rsid":"rs779760634","trait_name":"Autosomal recessive nonsyndromic hearing loss 31","url":"https://www.mygenelog.com/ko/variants/rs779760634"},{"risk_tier":"standard","rsid":"rs78026734","trait_name":"Serum alkaline phosphatase levels","url":"https://www.mygenelog.com/ko/variants/rs78026734"}]}