{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/DGUOK","ko":"https://www.mygenelog.com/ko/api/v1/genes/DGUOK"},"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":"DGUOK","url":"https://www.mygenelog.com/ko/genes/DGUOK","variant_count":26,"variants":[{"risk_tier":"sensitive","rsid":"rs104893630","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs104893630"},{"risk_tier":"sensitive","rsid":"rs104893631","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs104893631"},{"risk_tier":"sensitive","rsid":"rs104893632","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs104893632"},{"risk_tier":"sensitive","rsid":"rs104893633","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs104893633"},{"risk_tier":"sensitive","rsid":"rs1204316787","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs1204316787"},{"risk_tier":"sensitive","rsid":"rs1345120527","trait_name":"DGUOK-related disorder","url":"https://www.mygenelog.com/ko/variants/rs1345120527"},{"risk_tier":"sensitive","rsid":"rs140307681","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs140307681"},{"risk_tier":"sensitive","rsid":"rs150678946","trait_name":"DGUOK-related disorder","url":"https://www.mygenelog.com/ko/variants/rs150678946"},{"risk_tier":"sensitive","rsid":"rs2466942669","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs2466942669"},{"risk_tier":"sensitive","rsid":"rs2467050151","trait_name":"DGUOK-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2467050151"},{"risk_tier":"standard","rsid":"rs2694701","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs2694701"},{"risk_tier":"sensitive","rsid":"rs4852324","trait_name":"Systemic lupus erythematosus","url":"https://www.mygenelog.com/ko/variants/rs4852324"},{"risk_tier":"standard","rsid":"rs534297082","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","url":"https://www.mygenelog.com/ko/variants/rs534297082"},{"risk_tier":"sensitive","rsid":"rs587780587","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs587780587"},{"risk_tier":"sensitive","rsid":"rs6705628","trait_name":"Systemic lupus erythematosus","url":"https://www.mygenelog.com/ko/variants/rs6705628"},{"risk_tier":"standard","rsid":"rs748597500","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","url":"https://www.mygenelog.com/ko/variants/rs748597500"},{"risk_tier":"standard","rsid":"rs74874677","trait_name":"Mitochondrial DNA heteroplasmy (chrM:16183:AC:A case-only heteroplasmy)","url":"https://www.mygenelog.com/ko/variants/rs74874677"},{"risk_tier":"sensitive","rsid":"rs749464475","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs749464475"},{"risk_tier":"sensitive","rsid":"rs757874547","trait_name":"DGUOK-related disorder","url":"https://www.mygenelog.com/ko/variants/rs757874547"},{"risk_tier":"standard","rsid":"rs762550967","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","url":"https://www.mygenelog.com/ko/variants/rs762550967"},{"risk_tier":"standard","rsid":"rs763615602","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","url":"https://www.mygenelog.com/ko/variants/rs763615602"},{"risk_tier":"sensitive","rsid":"rs767604650","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs767604650"},{"risk_tier":"sensitive","rsid":"rs770950831","trait_name":"DGUOK-related disorder","url":"https://www.mygenelog.com/ko/variants/rs770950831"},{"risk_tier":"standard","rsid":"rs879255617","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","url":"https://www.mygenelog.com/ko/variants/rs879255617"},{"risk_tier":"sensitive","rsid":"rs886037846","trait_name":"Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)","url":"https://www.mygenelog.com/ko/variants/rs886037846"},{"risk_tier":"standard","rsid":"rs940941896","trait_name":"Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4","url":"https://www.mygenelog.com/ko/variants/rs940941896"}]}