{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/RDX","ko":"https://www.mygenelog.com/ko/api/v1/genes/RDX"},"condition_count":3,"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":"RDX","url":"https://www.mygenelog.com/genes/RDX","variant_count":16,"variants":[{"risk_tier":"sensitive","rsid":"rs10488763","trait_name":"Coronary artery disease","url":"https://www.mygenelog.com/variants/rs10488763"},{"risk_tier":"standard","rsid":"rs1191259480","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs1191259480"},{"risk_tier":"standard","rsid":"rs121918379","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs121918379"},{"risk_tier":"standard","rsid":"rs121918380","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs121918380"},{"risk_tier":"standard","rsid":"rs12361711","trait_name":"Putamen iron levels (R2* MRI)","url":"https://www.mygenelog.com/variants/rs12361711"},{"risk_tier":"standard","rsid":"rs1308348441","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs1308348441"},{"risk_tier":"standard","rsid":"rs1412883921","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs1412883921"},{"risk_tier":"standard","rsid":"rs1463925107","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs1463925107"},{"risk_tier":"standard","rsid":"rs2539441210","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs2539441210"},{"risk_tier":"sensitive","rsid":"rs550826317","trait_name":"Type 1 diabetes with renal manifestations (PheCode 250.12)","url":"https://www.mygenelog.com/variants/rs550826317"},{"risk_tier":"standard","rsid":"rs559056188","trait_name":"Pulmonary insufficiency or respiratory failure following trauma and surgery (PheCode 509.3)","url":"https://www.mygenelog.com/variants/rs559056188"},{"risk_tier":"standard","rsid":"rs630839","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs630839"},{"risk_tier":"standard","rsid":"rs7128556","trait_name":"High-density lipoprotein levels","url":"https://www.mygenelog.com/variants/rs7128556"},{"risk_tier":"standard","rsid":"rs756407279","trait_name":"Nonsyndromic genetic hearing loss","url":"https://www.mygenelog.com/variants/rs756407279"},{"risk_tier":"standard","rsid":"rs772146113","trait_name":"Autosomal recessive nonsyndromic hearing loss 24","url":"https://www.mygenelog.com/variants/rs772146113"},{"risk_tier":"standard","rsid":"rs7932082","trait_name":"Thalamus iron levels (quantitative susceptibility mapping)","url":"https://www.mygenelog.com/variants/rs7932082"}]}