{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SLC25A46","ko":"https://www.mygenelog.com/ko/api/v1/genes/SLC25A46"},"condition_count":2,"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":"SLC25A46","url":"https://www.mygenelog.com/ko/genes/SLC25A46","variant_count":24,"variants":[{"risk_tier":"standard","rsid":"rs10055042","trait_name":"Medication use (antihistamines for systemic use)","url":"https://www.mygenelog.com/ko/variants/rs10055042"},{"risk_tier":"standard","rsid":"rs10056243","trait_name":"Asthma","url":"https://www.mygenelog.com/ko/variants/rs10056243"},{"risk_tier":"standard","rsid":"rs1057518748","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1057518748"},{"risk_tier":"standard","rsid":"rs1057518750","trait_name":"Pontocerebellar hypoplasia, type 1E","url":"https://www.mygenelog.com/ko/variants/rs1057518750"},{"risk_tier":"standard","rsid":"rs1057519294","trait_name":"Pontocerebellar hypoplasia, type 1E","url":"https://www.mygenelog.com/ko/variants/rs1057519294"},{"risk_tier":"standard","rsid":"rs1057519295","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1057519295"},{"risk_tier":"standard","rsid":"rs1057519296","trait_name":"Pontocerebellar hypoplasia, type 1E","url":"https://www.mygenelog.com/ko/variants/rs1057519296"},{"risk_tier":"standard","rsid":"rs1171977270","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1171977270"},{"risk_tier":"standard","rsid":"rs1184021143","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1184021143"},{"risk_tier":"standard","rsid":"rs1278362025","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1278362025"},{"risk_tier":"standard","rsid":"rs1554093168","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1554093168"},{"risk_tier":"standard","rsid":"rs1561602892","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1561602892"},{"risk_tier":"standard","rsid":"rs1799815535","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1799815535"},{"risk_tier":"standard","rsid":"rs1799819389","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs1799819389"},{"risk_tier":"sensitive","rsid":"rs1814576","trait_name":"Allergic disease (asthma, hay fever or eczema)","url":"https://www.mygenelog.com/ko/variants/rs1814576"},{"risk_tier":"standard","rsid":"rs2547519976","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs2547519976"},{"risk_tier":"standard","rsid":"rs2547522906","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs2547522906"},{"risk_tier":"standard","rsid":"rs3853750","trait_name":"Asthma","url":"https://www.mygenelog.com/ko/variants/rs3853750"},{"risk_tier":"standard","rsid":"rs6893213","trait_name":"Asthma","url":"https://www.mygenelog.com/ko/variants/rs6893213"},{"risk_tier":"standard","rsid":"rs746681765","trait_name":"Neuropathy, hereditary motor and sensory, type 6B","url":"https://www.mygenelog.com/ko/variants/rs746681765"},{"risk_tier":"standard","rsid":"rs751101419","trait_name":"Pontocerebellar hypoplasia, type 1E","url":"https://www.mygenelog.com/ko/variants/rs751101419"},{"risk_tier":"standard","rsid":"rs771761288","trait_name":"Pontocerebellar hypoplasia, type 1E","url":"https://www.mygenelog.com/ko/variants/rs771761288"},{"risk_tier":"standard","rsid":"rs7734635","trait_name":"Asthma","url":"https://www.mygenelog.com/ko/variants/rs7734635"},{"risk_tier":"standard","rsid":"rs7735519","trait_name":"Medication use (adrenergics, inhalants)","url":"https://www.mygenelog.com/ko/variants/rs7735519"}]}