{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SETD1A","ko":"https://www.mygenelog.com/ko/api/v1/genes/SETD1A"},"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":"SETD1A","url":"https://www.mygenelog.com/genes/SETD1A","variant_count":19,"variants":[{"risk_tier":"sensitive","rsid":"rs1870293","trait_name":"Parkinson's disease","url":"https://www.mygenelog.com/variants/rs1870293"},{"risk_tier":"standard","rsid":"rs2056003750","trait_name":"Epilepsy, early-onset, with or without developmental delay","url":"https://www.mygenelog.com/variants/rs2056003750"},{"risk_tier":"sensitive","rsid":"rs2056099559","trait_name":"Schizophrenia","url":"https://www.mygenelog.com/variants/rs2056099559"},{"risk_tier":"standard","rsid":"rs2056100951","trait_name":"Epilepsy, early-onset, with or without developmental delay","url":"https://www.mygenelog.com/variants/rs2056100951"},{"risk_tier":"sensitive","rsid":"rs2056158149","trait_name":"Neurodevelopmental disorder with speech impairment and dysmorphic facies","url":"https://www.mygenelog.com/variants/rs2056158149"},{"risk_tier":"standard","rsid":"rs2056165149","trait_name":"Epilepsy, early-onset, with or without developmental delay","url":"https://www.mygenelog.com/variants/rs2056165149"},{"risk_tier":"sensitive","rsid":"rs2056360507","trait_name":"Neurodevelopmental disorder with speech impairment and dysmorphic facies","url":"https://www.mygenelog.com/variants/rs2056360507"},{"risk_tier":"standard","rsid":"rs2143509708","trait_name":"Epilepsy, early-onset, with or without developmental delay","url":"https://www.mygenelog.com/variants/rs2143509708"},{"risk_tier":"sensitive","rsid":"rs2543833500","trait_name":"Neurodevelopmental disorder with speech impairment and dysmorphic facies","url":"https://www.mygenelog.com/variants/rs2543833500"},{"risk_tier":"sensitive","rsid":"rs2543847896","trait_name":"Neurodevelopmental disorder with speech impairment and dysmorphic facies","url":"https://www.mygenelog.com/variants/rs2543847896"},{"risk_tier":"sensitive","rsid":"rs2543859166","trait_name":"Neurodevelopmental disorder with speech impairment and dysmorphic facies","url":"https://www.mygenelog.com/variants/rs2543859166"},{"risk_tier":"sensitive","rsid":"rs2543861155","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2543861155"},{"risk_tier":"sensitive","rsid":"rs2543909603","trait_name":"Neurodevelopmental disorder with speech impairment and dysmorphic facies","url":"https://www.mygenelog.com/variants/rs2543909603"},{"risk_tier":"standard","rsid":"rs4346218","trait_name":"Psoriasis (PheCode 696.4)","url":"https://www.mygenelog.com/variants/rs4346218"},{"risk_tier":"standard","rsid":"rs61744449","trait_name":"Epilepsy, early-onset, with or without developmental delay","url":"https://www.mygenelog.com/variants/rs61744449"},{"risk_tier":"sensitive","rsid":"rs770913157","trait_name":"Schizophrenia","url":"https://www.mygenelog.com/variants/rs770913157"},{"risk_tier":"standard","rsid":"rs781482552","trait_name":"Epilepsy, early-onset, with or without developmental delay","url":"https://www.mygenelog.com/variants/rs781482552"},{"risk_tier":"sensitive","rsid":"rs869312829","trait_name":"Schizophrenia","url":"https://www.mygenelog.com/variants/rs869312829"},{"risk_tier":"sensitive","rsid":"rs869312831","trait_name":"Schizophrenia","url":"https://www.mygenelog.com/variants/rs869312831"}]}