{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/FLVCR1","ko":"https://www.mygenelog.com/ko/api/v1/genes/FLVCR1"},"condition_count":4,"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":"FLVCR1","url":"https://www.mygenelog.com/ko/genes/FLVCR1","variant_count":19,"variants":[{"risk_tier":"standard","rsid":"rs12408694","trait_name":"Hemoglobin levels","url":"https://www.mygenelog.com/ko/variants/rs12408694"},{"risk_tier":"standard","rsid":"rs1315527384","trait_name":"Retinitis pigmentosa","url":"https://www.mygenelog.com/ko/variants/rs1315527384"},{"risk_tier":"sensitive","rsid":"rs1468358104","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1468358104"},{"risk_tier":"standard","rsid":"rs1558104145","trait_name":"Jeune thoracic dystrophy","url":"https://www.mygenelog.com/ko/variants/rs1558104145"},{"risk_tier":"standard","rsid":"rs1558112968","trait_name":"Retinitis pigmentosa","url":"https://www.mygenelog.com/ko/variants/rs1558112968"},{"risk_tier":"sensitive","rsid":"rs1558121050","trait_name":"Posterior column ataxia-retinitis pigmentosa syndrome","url":"https://www.mygenelog.com/ko/variants/rs1558121050"},{"risk_tier":"standard","rsid":"rs1664140651","trait_name":"Retinitis pigmentosa","url":"https://www.mygenelog.com/ko/variants/rs1664140651"},{"risk_tier":"standard","rsid":"rs2047287","trait_name":"RBC levels of Choline","url":"https://www.mygenelog.com/ko/variants/rs2047287"},{"risk_tier":"standard","rsid":"rs2359324","trait_name":"Hematocrit","url":"https://www.mygenelog.com/ko/variants/rs2359324"},{"risk_tier":"sensitive","rsid":"rs2464385404","trait_name":"Posterior column ataxia-retinitis pigmentosa syndrome","url":"https://www.mygenelog.com/ko/variants/rs2464385404"},{"risk_tier":"sensitive","rsid":"rs267606819","trait_name":"Posterior column ataxia-retinitis pigmentosa syndrome","url":"https://www.mygenelog.com/ko/variants/rs267606819"},{"risk_tier":"sensitive","rsid":"rs267606820","trait_name":"Posterior column ataxia-retinitis pigmentosa syndrome","url":"https://www.mygenelog.com/ko/variants/rs267606820"},{"risk_tier":"sensitive","rsid":"rs267606821","trait_name":"Posterior column ataxia-retinitis pigmentosa syndrome","url":"https://www.mygenelog.com/ko/variants/rs267606821"},{"risk_tier":"sensitive","rsid":"rs372728084","trait_name":"Posterior column ataxia-retinitis pigmentosa syndrome","url":"https://www.mygenelog.com/ko/variants/rs372728084"},{"risk_tier":"standard","rsid":"rs556788423","trait_name":"Retinal dystrophy","url":"https://www.mygenelog.com/ko/variants/rs556788423"},{"risk_tier":"sensitive","rsid":"rs746482522","trait_name":"FLVCR1-related disorders","url":"https://www.mygenelog.com/ko/variants/rs746482522"},{"risk_tier":"sensitive","rsid":"rs777525949","trait_name":"FLVCR1-related disorders","url":"https://www.mygenelog.com/ko/variants/rs777525949"},{"risk_tier":"sensitive","rsid":"rs899735028","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs899735028"},{"risk_tier":"standard","rsid":"rs963327","trait_name":"Hemoglobin concentration","url":"https://www.mygenelog.com/ko/variants/rs963327"}]}