{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/ATP1A1","ko":"https://www.mygenelog.com/ko/api/v1/genes/ATP1A1"},"condition_count":1,"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":"ATP1A1","url":"https://www.mygenelog.com/genes/ATP1A1","variant_count":14,"variants":[{"risk_tier":"standard","rsid":"rs12087680","trait_name":"White blood cell count","url":"https://www.mygenelog.com/variants/rs12087680"},{"risk_tier":"sensitive","rsid":"rs1553190285","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs1553190285"},{"risk_tier":"sensitive","rsid":"rs1553192086","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs1553192086"},{"risk_tier":"sensitive","rsid":"rs1553192091","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs1553192091"},{"risk_tier":"standard","rsid":"rs1557785499","trait_name":"Hypomagnesemia, seizures, and intellectual disability 2","url":"https://www.mygenelog.com/variants/rs1557785499"},{"risk_tier":"standard","rsid":"rs1557785503","trait_name":"Hypomagnesemia, seizures, and intellectual disability 2","url":"https://www.mygenelog.com/variants/rs1557785503"},{"risk_tier":"standard","rsid":"rs1570980551","trait_name":"Hypomagnesemia, seizures, and intellectual disability 2","url":"https://www.mygenelog.com/variants/rs1570980551"},{"risk_tier":"sensitive","rsid":"rs1653241392","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs1653241392"},{"risk_tier":"sensitive","rsid":"rs2101045655","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs2101045655"},{"risk_tier":"sensitive","rsid":"rs2101052251","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs2101052251"},{"risk_tier":"sensitive","rsid":"rs2101055022","trait_name":"Charcot-Marie-tooth disease, axonal, type 2DD","url":"https://www.mygenelog.com/variants/rs2101055022"},{"risk_tier":"sensitive","rsid":"rs2101066493","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2101066493"},{"risk_tier":"standard","rsid":"rs61788009","trait_name":"Hip index","url":"https://www.mygenelog.com/variants/rs61788009"},{"risk_tier":"standard","rsid":"rs781629728","trait_name":"Hypomagnesemia, seizures, and intellectual disability 2","url":"https://www.mygenelog.com/variants/rs781629728"}]}