{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SLC25A4","ko":"https://www.mygenelog.com/ko/api/v1/genes/SLC25A4"},"condition_count":0,"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":"SLC25A4","url":"https://www.mygenelog.com/ko/genes/SLC25A4","variant_count":10,"variants":[{"risk_tier":"standard","rsid":"rs104893873","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2","url":"https://www.mygenelog.com/ko/variants/rs104893873"},{"risk_tier":"standard","rsid":"rs104893874","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2","url":"https://www.mygenelog.com/ko/variants/rs104893874"},{"risk_tier":"standard","rsid":"rs104893876","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2","url":"https://www.mygenelog.com/ko/variants/rs104893876"},{"risk_tier":"sensitive","rsid":"rs121912683","trait_name":"Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive","url":"https://www.mygenelog.com/ko/variants/rs121912683"},{"risk_tier":"sensitive","rsid":"rs1560841701","trait_name":"Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs1560841701"},{"risk_tier":"standard","rsid":"rs28999114","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2","url":"https://www.mygenelog.com/ko/variants/rs28999114"},{"risk_tier":"sensitive","rsid":"rs398122942","trait_name":"Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive","url":"https://www.mygenelog.com/ko/variants/rs398122942"},{"risk_tier":"sensitive","rsid":"rs770816416","trait_name":"Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive","url":"https://www.mygenelog.com/ko/variants/rs770816416"},{"risk_tier":"sensitive","rsid":"rs886041081","trait_name":"Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs886041081"},{"risk_tier":"sensitive","rsid":"rs886041082","trait_name":"Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant","url":"https://www.mygenelog.com/ko/variants/rs886041082"}]}