{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/CLRN1","ko":"https://www.mygenelog.com/ko/api/v1/genes/CLRN1"},"condition_count":4,"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":"CLRN1","url":"https://www.mygenelog.com/genes/CLRN1","variant_count":35,"variants":[{"risk_tier":"sensitive","rsid":"rs1057517224","trait_name":"Usher syndrome type 3A","url":"https://www.mygenelog.com/variants/rs1057517224"},{"risk_tier":"sensitive","rsid":"rs111033258","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs111033258"},{"risk_tier":"sensitive","rsid":"rs111033267","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs111033267"},{"risk_tier":"sensitive","rsid":"rs121908140","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs121908140"},{"risk_tier":"sensitive","rsid":"rs121908141","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs121908141"},{"risk_tier":"sensitive","rsid":"rs121908142","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs121908142"},{"risk_tier":"standard","rsid":"rs1287122500","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs1287122500"},{"risk_tier":"standard","rsid":"rs1329440649","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs1329440649"},{"risk_tier":"sensitive","rsid":"rs1380661508","trait_name":"Usher syndrome","url":"https://www.mygenelog.com/variants/rs1380661508"},{"risk_tier":"standard","rsid":"rs1463067573","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs1463067573"},{"risk_tier":"sensitive","rsid":"rs1553776112","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs1553776112"},{"risk_tier":"sensitive","rsid":"rs1559982739","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs1559982739"},{"risk_tier":"sensitive","rsid":"rs1576651623","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs1576651623"},{"risk_tier":"sensitive","rsid":"rs1712936705","trait_name":"CLRN1-related disorder","url":"https://www.mygenelog.com/variants/rs1712936705"},{"risk_tier":"sensitive","rsid":"rs1713861377","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs1713861377"},{"risk_tier":"sensitive","rsid":"rs1715589813","trait_name":"Usher syndrome type 3A","url":"https://www.mygenelog.com/variants/rs1715589813"},{"risk_tier":"standard","rsid":"rs1715594024","trait_name":"Neuronal ceroid lipofuscinosis","url":"https://www.mygenelog.com/variants/rs1715594024"},{"risk_tier":"sensitive","rsid":"rs201205811","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs201205811"},{"risk_tier":"sensitive","rsid":"rs201625237","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs201625237"},{"risk_tier":"sensitive","rsid":"rs2107927490","trait_name":"Usher syndrome type 3A","url":"https://www.mygenelog.com/variants/rs2107927490"},{"risk_tier":"sensitive","rsid":"rs2107927808","trait_name":"Usher syndrome","url":"https://www.mygenelog.com/variants/rs2107927808"},{"risk_tier":"standard","rsid":"rs2472761635","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs2472761635"},{"risk_tier":"standard","rsid":"rs2472830632","trait_name":"Retinal dystrophy","url":"https://www.mygenelog.com/variants/rs2472830632"},{"risk_tier":"standard","rsid":"rs2472831349","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs2472831349"},{"risk_tier":"sensitive","rsid":"rs373208120","trait_name":"Usher syndrome type 3A","url":"https://www.mygenelog.com/variants/rs373208120"},{"risk_tier":"standard","rsid":"rs374390376","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs374390376"},{"risk_tier":"sensitive","rsid":"rs374963432","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs374963432"},{"risk_tier":"sensitive","rsid":"rs376155416","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs376155416"},{"risk_tier":"standard","rsid":"rs745585873","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs745585873"},{"risk_tier":"sensitive","rsid":"rs758741442","trait_name":"Usher syndrome type 3A","url":"https://www.mygenelog.com/variants/rs758741442"},{"risk_tier":"standard","rsid":"rs7649164","trait_name":"Chronotype","url":"https://www.mygenelog.com/variants/rs7649164"},{"risk_tier":"standard","rsid":"rs775098953","trait_name":"Retinitis pigmentosa 61","url":"https://www.mygenelog.com/variants/rs775098953"},{"risk_tier":"standard","rsid":"rs878853379","trait_name":"Retinal dystrophy","url":"https://www.mygenelog.com/variants/rs878853379"},{"risk_tier":"sensitive","rsid":"rs933370216","trait_name":"Usher syndrome type 3","url":"https://www.mygenelog.com/variants/rs933370216"},{"risk_tier":"sensitive","rsid":"rs976853535","trait_name":"CLRN1-related disorder","url":"https://www.mygenelog.com/variants/rs976853535"}]}
