{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/UBE3B","ko":"https://www.mygenelog.com/ko/api/v1/genes/UBE3B"},"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":"UBE3B","url":"https://www.mygenelog.com/genes/UBE3B","variant_count":30,"variants":[{"risk_tier":"sensitive","rsid":"rs1037348200","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs1037348200"},{"risk_tier":"standard","rsid":"rs10744826","trait_name":"High density lipoprotein cholesterol levels","url":"https://www.mygenelog.com/variants/rs10744826"},{"risk_tier":"sensitive","rsid":"rs1304422857","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1304422857"},{"risk_tier":"sensitive","rsid":"rs1555269815","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs1555269815"},{"risk_tier":"sensitive","rsid":"rs1558803","trait_name":"Coronary artery disease","url":"https://www.mygenelog.com/variants/rs1558803"},{"risk_tier":"sensitive","rsid":"rs1566078009","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs1566078009"},{"risk_tier":"sensitive","rsid":"rs1592882265","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs1592882265"},{"risk_tier":"standard","rsid":"rs2004359","trait_name":"PR interval","url":"https://www.mygenelog.com/variants/rs2004359"},{"risk_tier":"sensitive","rsid":"rs2135832115","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs2135832115"},{"risk_tier":"sensitive","rsid":"rs2136063413","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs2136063413"},{"risk_tier":"sensitive","rsid":"rs2136067033","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs2136067033"},{"risk_tier":"standard","rsid":"rs2241208","trait_name":"High density lipoprotein cholesterol levels","url":"https://www.mygenelog.com/variants/rs2241208"},{"risk_tier":"standard","rsid":"rs2241212","trait_name":"Total cholesterol levels","url":"https://www.mygenelog.com/variants/rs2241212"},{"risk_tier":"sensitive","rsid":"rs2548532884","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs2548532884"},{"risk_tier":"sensitive","rsid":"rs2548543775","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs2548543775"},{"risk_tier":"sensitive","rsid":"rs2548565787","trait_name":"Blepharophimosis - intellectual disability syndrome","url":"https://www.mygenelog.com/variants/rs2548565787"},{"risk_tier":"sensitive","rsid":"rs398123020","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs398123020"},{"risk_tier":"sensitive","rsid":"rs398123022","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs398123022"},{"risk_tier":"sensitive","rsid":"rs398123023","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs398123023"},{"risk_tier":"sensitive","rsid":"rs539407162","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs539407162"},{"risk_tier":"standard","rsid":"rs7311187","trait_name":"Free cholesterol in very large HDL","url":"https://www.mygenelog.com/variants/rs7311187"},{"risk_tier":"sensitive","rsid":"rs746058354","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs746058354"},{"risk_tier":"sensitive","rsid":"rs748637278","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs748637278"},{"risk_tier":"sensitive","rsid":"rs750360032","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs750360032"},{"risk_tier":"sensitive","rsid":"rs761700377","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs761700377"},{"risk_tier":"sensitive","rsid":"rs775981553","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs775981553"},{"risk_tier":"standard","rsid":"rs78235098","trait_name":"Diastolic blood pressure (MTAG)","url":"https://www.mygenelog.com/variants/rs78235098"},{"risk_tier":"sensitive","rsid":"rs918170054","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs918170054"},{"risk_tier":"sensitive","rsid":"rs934035216","trait_name":"UBE3B-related disorder","url":"https://www.mygenelog.com/variants/rs934035216"},{"risk_tier":"sensitive","rsid":"rs989411551","trait_name":"Oculocerebrofacial syndrome, Kaufman type","url":"https://www.mygenelog.com/variants/rs989411551"}]}