{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SOX10","ko":"https://www.mygenelog.com/ko/api/v1/genes/SOX10"},"condition_count":5,"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":"SOX10","url":"https://www.mygenelog.com/genes/SOX10","variant_count":56,"variants":[{"risk_tier":"sensitive","rsid":"rs1057518656","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1057518656"},{"risk_tier":"sensitive","rsid":"rs1164043046","trait_name":"Waardenburg syndrome","url":"https://www.mygenelog.com/variants/rs1164043046"},{"risk_tier":"sensitive","rsid":"rs121909117","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs121909117"},{"risk_tier":"sensitive","rsid":"rs1373797370","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs1373797370"},{"risk_tier":"sensitive","rsid":"rs1482985217","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1482985217"},{"risk_tier":"standard","rsid":"rs149871701","trait_name":"Mean spheric corpuscular volume","url":"https://www.mygenelog.com/variants/rs149871701"},{"risk_tier":"sensitive","rsid":"rs1555937400","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs1555937400"},{"risk_tier":"sensitive","rsid":"rs1555938395","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1555938395"},{"risk_tier":"standard","rsid":"rs1555939403","trait_name":"Rare genetic deafness","url":"https://www.mygenelog.com/variants/rs1555939403"},{"risk_tier":"standard","rsid":"rs1555939408","trait_name":"Rare genetic deafness","url":"https://www.mygenelog.com/variants/rs1555939408"},{"risk_tier":"sensitive","rsid":"rs1555939415","trait_name":"Waardenburg syndrome type 2A","url":"https://www.mygenelog.com/variants/rs1555939415"},{"risk_tier":"sensitive","rsid":"rs1555939426","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs1555939426"},{"risk_tier":"sensitive","rsid":"rs1555939459","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs1555939459"},{"risk_tier":"sensitive","rsid":"rs1555939491","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1555939491"},{"risk_tier":"sensitive","rsid":"rs1555939523","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs1555939523"},{"risk_tier":"sensitive","rsid":"rs1569169289","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1569169289"},{"risk_tier":"sensitive","rsid":"rs1569169328","trait_name":"Waardenburg syndrome type 4A","url":"https://www.mygenelog.com/variants/rs1569169328"},{"risk_tier":"sensitive","rsid":"rs1601886662","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1601886662"},{"risk_tier":"sensitive","rsid":"rs1932130190","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932130190"},{"risk_tier":"sensitive","rsid":"rs1932137446","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932137446"},{"risk_tier":"sensitive","rsid":"rs1932142815","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs1932142815"},{"risk_tier":"sensitive","rsid":"rs1932279377","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932279377"},{"risk_tier":"sensitive","rsid":"rs1932280017","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932280017"},{"risk_tier":"sensitive","rsid":"rs1932460904","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932460904"},{"risk_tier":"sensitive","rsid":"rs1932462410","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932462410"},{"risk_tier":"sensitive","rsid":"rs1932463755","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932463755"},{"risk_tier":"sensitive","rsid":"rs1932463844","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932463844"},{"risk_tier":"sensitive","rsid":"rs1932464388","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932464388"},{"risk_tier":"sensitive","rsid":"rs1932477493","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs1932477493"},{"risk_tier":"sensitive","rsid":"rs1932482365","trait_name":"Waardenburg syndrome type 2E","url":"https://www.mygenelog.com/variants/rs1932482365"},{"risk_tier":"sensitive","rsid":"rs2145760379","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs2145760379"},{"risk_tier":"sensitive","rsid":"rs2145761680","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs2145761680"},{"risk_tier":"sensitive","rsid":"rs2145768136","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs2145768136"},{"risk_tier":"sensitive","rsid":"rs2145768481","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs2145768481"},{"risk_tier":"standard","rsid":"rs2145768544","trait_name":"Deafness with anatomical inner ear anomalies","url":"https://www.mygenelog.com/variants/rs2145768544"},{"risk_tier":"sensitive","rsid":"rs2145776911","trait_name":"Waardenburg syndrome type 1","url":"https://www.mygenelog.com/variants/rs2145776911"},{"risk_tier":"sensitive","rsid":"rs2145776948","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs2145776948"},{"risk_tier":"sensitive","rsid":"rs2145776981","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs2145776981"},{"risk_tier":"sensitive","rsid":"rs2145777042","trait_name":"Waardenburg syndrome type 1","url":"https://www.mygenelog.com/variants/rs2145777042"},{"risk_tier":"sensitive","rsid":"rs2518046893","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs2518046893"},{"risk_tier":"sensitive","rsid":"rs267607081","trait_name":"Waardenburg syndrome type 2E, with neurologic involvement","url":"https://www.mygenelog.com/variants/rs267607081"},{"risk_tier":"sensitive","rsid":"rs281797260","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs281797260"},{"risk_tier":"sensitive","rsid":"rs397515370","trait_name":"Waardenburg syndrome type 2E, with neurologic involvement","url":"https://www.mygenelog.com/variants/rs397515370"},{"risk_tier":"sensitive","rsid":"rs397515457","trait_name":"Waardenburg syndrome type 2E, without neurologic involvement","url":"https://www.mygenelog.com/variants/rs397515457"},{"risk_tier":"sensitive","rsid":"rs606231342","trait_name":"Hirschsprung disease, susceptibility to, 1","url":"https://www.mygenelog.com/variants/rs606231342"},{"risk_tier":"sensitive","rsid":"rs73415876","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs73415876"},{"risk_tier":"sensitive","rsid":"rs74315514","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs74315514"},{"risk_tier":"sensitive","rsid":"rs74315515","trait_name":"Waardenburg syndrome type 2E, without neurologic involvement","url":"https://www.mygenelog.com/variants/rs74315515"},{"risk_tier":"sensitive","rsid":"rs74315516","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs74315516"},{"risk_tier":"sensitive","rsid":"rs74315518","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs74315518"},{"risk_tier":"sensitive","rsid":"rs74315520","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs74315520"},{"risk_tier":"sensitive","rsid":"rs74315521","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs74315521"},{"risk_tier":"sensitive","rsid":"rs756120041","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs756120041"},{"risk_tier":"sensitive","rsid":"rs763210407","trait_name":"Waardenburg syndrome type 4C","url":"https://www.mygenelog.com/variants/rs763210407"},{"risk_tier":"standard","rsid":"rs876657660","trait_name":"Rare genetic deafness","url":"https://www.mygenelog.com/variants/rs876657660"},{"risk_tier":"sensitive","rsid":"rs886039664","trait_name":"PCWH syndrome","url":"https://www.mygenelog.com/variants/rs886039664"}]}