{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/ITPR1","ko":"https://www.mygenelog.com/ko/api/v1/genes/ITPR1"},"condition_count":8,"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":"ITPR1","url":"https://www.mygenelog.com/ko/genes/ITPR1","variant_count":57,"variants":[{"risk_tier":"sensitive","rsid":"rs1064796252","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1064796252"},{"risk_tier":"sensitive","rsid":"rs1064796337","trait_name":"ITPR1-related disorders","url":"https://www.mygenelog.com/ko/variants/rs1064796337"},{"risk_tier":"sensitive","rsid":"rs1085308010","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1085308010"},{"risk_tier":"standard","rsid":"rs1114167316","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs1114167316"},{"risk_tier":"sensitive","rsid":"rs1131691919","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs1131691919"},{"risk_tier":"standard","rsid":"rs116654145","trait_name":"Protozoan infection (PheCode 131)","url":"https://www.mygenelog.com/ko/variants/rs116654145"},{"risk_tier":"standard","rsid":"rs121912425","trait_name":"Spinocerebellar ataxia type 15/16","url":"https://www.mygenelog.com/ko/variants/rs121912425"},{"risk_tier":"standard","rsid":"rs1322796318","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs1322796318"},{"risk_tier":"standard","rsid":"rs13313995","trait_name":"Male-pattern baldness","url":"https://www.mygenelog.com/ko/variants/rs13313995"},{"risk_tier":"standard","rsid":"rs138057778","trait_name":"RBC levels of Sphingosine 1-phosphate","url":"https://www.mygenelog.com/ko/variants/rs138057778"},{"risk_tier":"standard","rsid":"rs143184903","trait_name":"Number of pure reticular pseudodrusen","url":"https://www.mygenelog.com/ko/variants/rs143184903"},{"risk_tier":"standard","rsid":"rs1443276640","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs1443276640"},{"risk_tier":"sensitive","rsid":"rs1553666546","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1553666546"},{"risk_tier":"sensitive","rsid":"rs1553681758","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1553681758"},{"risk_tier":"standard","rsid":"rs1553756062","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs1553756062"},{"risk_tier":"sensitive","rsid":"rs1553758021","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs1553758021"},{"risk_tier":"sensitive","rsid":"rs1559638068","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs1559638068"},{"risk_tier":"standard","rsid":"rs1559718601","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs1559718601"},{"risk_tier":"standard","rsid":"rs17041517","trait_name":"Sarcoidosis","url":"https://www.mygenelog.com/ko/variants/rs17041517"},{"risk_tier":"sensitive","rsid":"rs2046415471","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs2046415471"},{"risk_tier":"standard","rsid":"rs2054872","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs2054872"},{"risk_tier":"standard","rsid":"rs2093873520","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs2093873520"},{"risk_tier":"standard","rsid":"rs2093873570","trait_name":"Spinocerebellar ataxia type 15/16","url":"https://www.mygenelog.com/ko/variants/rs2093873570"},{"risk_tier":"standard","rsid":"rs2093873717","trait_name":"Intellectual disability","url":"https://www.mygenelog.com/ko/variants/rs2093873717"},{"risk_tier":"standard","rsid":"rs2106494596","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs2106494596"},{"risk_tier":"standard","rsid":"rs2125159664","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs2125159664"},{"risk_tier":"standard","rsid":"rs2125159710","trait_name":"Spinocerebellar ataxia type 15/16","url":"https://www.mygenelog.com/ko/variants/rs2125159710"},{"risk_tier":"standard","rsid":"rs2125193560","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs2125193560"},{"risk_tier":"standard","rsid":"rs2125201841","trait_name":"Spinocerebellar ataxia type 15/16","url":"https://www.mygenelog.com/ko/variants/rs2125201841"},{"risk_tier":"standard","rsid":"rs2125272771","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs2125272771"},{"risk_tier":"standard","rsid":"rs2469953279","trait_name":"Bilateral congenital mydriasis","url":"https://www.mygenelog.com/ko/variants/rs2469953279"},{"risk_tier":"standard","rsid":"rs2470706402","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs2470706402"},{"risk_tier":"standard","rsid":"rs34758081","trait_name":"Free Cholesterol to Cholesteryl Esters in Very Large HDL ratio","url":"https://www.mygenelog.com/ko/variants/rs34758081"},{"risk_tier":"standard","rsid":"rs35154162","trait_name":"Calcium levels","url":"https://www.mygenelog.com/ko/variants/rs35154162"},{"risk_tier":"standard","rsid":"rs397514535","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs397514535"},{"risk_tier":"standard","rsid":"rs397514536","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs397514536"},{"risk_tier":"standard","rsid":"rs4684433","trait_name":"Uterine fibroids","url":"https://www.mygenelog.com/ko/variants/rs4684433"},{"risk_tier":"standard","rsid":"rs569811612","trait_name":"LRRN1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs569811612"},{"risk_tier":"sensitive","rsid":"rs6762644","trait_name":"Breast cancer","url":"https://www.mygenelog.com/ko/variants/rs6762644"},{"risk_tier":"standard","rsid":"rs6786560","trait_name":"Sex hormone-binding globulin levels","url":"https://www.mygenelog.com/ko/variants/rs6786560"},{"risk_tier":"sensitive","rsid":"rs6787391","trait_name":"Breast cancer","url":"https://www.mygenelog.com/ko/variants/rs6787391"},{"risk_tier":"standard","rsid":"rs6792995","trait_name":"Gamma glutamyl transferase levels","url":"https://www.mygenelog.com/ko/variants/rs6792995"},{"risk_tier":"standard","rsid":"rs74829116","trait_name":"SETMAR protein levels","url":"https://www.mygenelog.com/ko/variants/rs74829116"},{"risk_tier":"sensitive","rsid":"rs752281590","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs752281590"},{"risk_tier":"standard","rsid":"rs79230762","trait_name":"Serum alkaline phosphatase levels","url":"https://www.mygenelog.com/ko/variants/rs79230762"},{"risk_tier":"sensitive","rsid":"rs797044955","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs797044955"},{"risk_tier":"standard","rsid":"rs863224882","trait_name":"Spinocerebellar ataxia type 29","url":"https://www.mygenelog.com/ko/variants/rs863224882"},{"risk_tier":"standard","rsid":"rs869312685","trait_name":"Spinocerebellar ataxia type 15/16","url":"https://www.mygenelog.com/ko/variants/rs869312685"},{"risk_tier":"sensitive","rsid":"rs878853171","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs878853171"},{"risk_tier":"sensitive","rsid":"rs878853172","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs878853172"},{"risk_tier":"sensitive","rsid":"rs878853173","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs878853173"},{"risk_tier":"sensitive","rsid":"rs878853174","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs878853174"},{"risk_tier":"sensitive","rsid":"rs878853176","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs878853176"},{"risk_tier":"sensitive","rsid":"rs878853177","trait_name":"Gillespie syndrome","url":"https://www.mygenelog.com/ko/variants/rs878853177"},{"risk_tier":"sensitive","rsid":"rs886039392","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs886039392"},{"risk_tier":"standard","rsid":"rs901850","trait_name":"Hand grip strength","url":"https://www.mygenelog.com/ko/variants/rs901850"},{"risk_tier":"standard","rsid":"rs9829279","trait_name":"Glutamine levels","url":"https://www.mygenelog.com/ko/variants/rs9829279"}]}