{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/KCNMA1","ko":"https://www.mygenelog.com/ko/api/v1/genes/KCNMA1"},"condition_count":12,"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":"KCNMA1","url":"https://www.mygenelog.com/ko/genes/KCNMA1","variant_count":35,"variants":[{"risk_tier":"standard","rsid":"rs10762738","trait_name":"Hypospadias","url":"https://www.mygenelog.com/ko/variants/rs10762738"},{"risk_tier":"standard","rsid":"rs10824516","trait_name":"Spherical equivalent","url":"https://www.mygenelog.com/ko/variants/rs10824516"},{"risk_tier":"standard","rsid":"rs11001967","trait_name":"Educational attainment","url":"https://www.mygenelog.com/ko/variants/rs11001967"},{"risk_tier":"standard","rsid":"rs11002137","trait_name":"Refractive error","url":"https://www.mygenelog.com/ko/variants/rs11002137"},{"risk_tier":"standard","rsid":"rs12415834","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs12415834"},{"risk_tier":"standard","rsid":"rs1247785","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs1247785"},{"risk_tier":"standard","rsid":"rs1248571","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs1248571"},{"risk_tier":"standard","rsid":"rs1328294721","trait_name":"Cerebellar atrophy, developmental delay, and seizures","url":"https://www.mygenelog.com/ko/variants/rs1328294721"},{"risk_tier":"sensitive","rsid":"rs137853333","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs137853333"},{"risk_tier":"standard","rsid":"rs150678882","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs150678882"},{"risk_tier":"sensitive","rsid":"rs1554829003","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1554829003"},{"risk_tier":"sensitive","rsid":"rs1554966197","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs1554966197"},{"risk_tier":"sensitive","rsid":"rs1565091862","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs1565091862"},{"risk_tier":"standard","rsid":"rs17407165","trait_name":"Refractive error","url":"https://www.mygenelog.com/ko/variants/rs17407165"},{"risk_tier":"standard","rsid":"rs17480656","trait_name":"Male-pattern baldness","url":"https://www.mygenelog.com/ko/variants/rs17480656"},{"risk_tier":"standard","rsid":"rs1873691","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs1873691"},{"risk_tier":"standard","rsid":"rs1877998","trait_name":"Heel bone mineral density","url":"https://www.mygenelog.com/ko/variants/rs1877998"},{"risk_tier":"sensitive","rsid":"rs2065361594","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs2065361594"},{"risk_tier":"standard","rsid":"rs2082415","trait_name":"Uterine leiomyomata","url":"https://www.mygenelog.com/ko/variants/rs2082415"},{"risk_tier":"sensitive","rsid":"rs2090875352","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs2090875352"},{"risk_tier":"sensitive","rsid":"rs2094531972","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs2094531972"},{"risk_tier":"standard","rsid":"rs2096271045","trait_name":"Cerebellar atrophy, developmental delay, and seizures","url":"https://www.mygenelog.com/ko/variants/rs2096271045"},{"risk_tier":"sensitive","rsid":"rs2116829","trait_name":"Restless legs syndrome","url":"https://www.mygenelog.com/ko/variants/rs2116829"},{"risk_tier":"standard","rsid":"rs2116830","trait_name":"Obesity","url":"https://www.mygenelog.com/ko/variants/rs2116830"},{"risk_tier":"sensitive","rsid":"rs2153792212","trait_name":"Liang-Wang syndrome","url":"https://www.mygenelog.com/ko/variants/rs2153792212"},{"risk_tier":"sensitive","rsid":"rs2153875876","trait_name":"Liang-Wang syndrome","url":"https://www.mygenelog.com/ko/variants/rs2153875876"},{"risk_tier":"sensitive","rsid":"rs2154251764","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs2154251764"},{"risk_tier":"sensitive","rsid":"rs2549038309","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs2549038309"},{"risk_tier":"sensitive","rsid":"rs2550658119","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs2550658119"},{"risk_tier":"sensitive","rsid":"rs2551714172","trait_name":"Autism spectrum disorder","url":"https://www.mygenelog.com/ko/variants/rs2551714172"},{"risk_tier":"standard","rsid":"rs4979905","trait_name":"Heel bone mineral density","url":"https://www.mygenelog.com/ko/variants/rs4979905"},{"risk_tier":"standard","rsid":"rs592676","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs592676"},{"risk_tier":"standard","rsid":"rs778732496","trait_name":"GLIPR1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs778732496"},{"risk_tier":"sensitive","rsid":"rs863224885","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs863224885"},{"risk_tier":"sensitive","rsid":"rs886039469","trait_name":"Generalized epilepsy-paroxysmal dyskinesia syndrome","url":"https://www.mygenelog.com/ko/variants/rs886039469"}]}