{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/OBSCN","ko":"https://www.mygenelog.com/ko/api/v1/genes/OBSCN"},"condition_count":5,"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":"OBSCN","url":"https://www.mygenelog.com/ko/genes/OBSCN","variant_count":16,"variants":[{"risk_tier":"standard","rsid":"rs116347362","trait_name":"GLIPR1 protein levels","url":"https://www.mygenelog.com/ko/variants/rs116347362"},{"risk_tier":"standard","rsid":"rs1757148","trait_name":"Atrial fibrillation","url":"https://www.mygenelog.com/ko/variants/rs1757148"},{"risk_tier":"standard","rsid":"rs200849058","trait_name":"Rhabdomyolysis, susceptibility to, 1","url":"https://www.mygenelog.com/ko/variants/rs200849058"},{"risk_tier":"sensitive","rsid":"rs2545712483","trait_name":"OBSCN-related disorder","url":"https://www.mygenelog.com/ko/variants/rs2545712483"},{"risk_tier":"standard","rsid":"rs287606","trait_name":"PR interval","url":"https://www.mygenelog.com/ko/variants/rs287606"},{"risk_tier":"standard","rsid":"rs287615","trait_name":"Impedance of arm right (UKB data field 23109)","url":"https://www.mygenelog.com/ko/variants/rs287615"},{"risk_tier":"standard","rsid":"rs3738685","trait_name":"JT interval","url":"https://www.mygenelog.com/ko/variants/rs3738685"},{"risk_tier":"standard","rsid":"rs397637","trait_name":"PR interval","url":"https://www.mygenelog.com/ko/variants/rs397637"},{"risk_tier":"standard","rsid":"rs417237","trait_name":"Estimated glomerular filtration rate","url":"https://www.mygenelog.com/ko/variants/rs417237"},{"risk_tier":"standard","rsid":"rs449133","trait_name":"WNT9A protein levels","url":"https://www.mygenelog.com/ko/variants/rs449133"},{"risk_tier":"standard","rsid":"rs4653943","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs4653943"},{"risk_tier":"standard","rsid":"rs500049","trait_name":"Creatinine levels","url":"https://www.mygenelog.com/ko/variants/rs500049"},{"risk_tier":"standard","rsid":"rs531253434","trait_name":"Rhabdomyolysis, susceptibility to, 1","url":"https://www.mygenelog.com/ko/variants/rs531253434"},{"risk_tier":"standard","rsid":"rs55756479","trait_name":"JT interval","url":"https://www.mygenelog.com/ko/variants/rs55756479"},{"risk_tier":"standard","rsid":"rs749025131","trait_name":"Hearing loss, autosomal recessive 120","url":"https://www.mygenelog.com/ko/variants/rs749025131"},{"risk_tier":"standard","rsid":"rs78529941","trait_name":"Right ventricular ejection fraction","url":"https://www.mygenelog.com/ko/variants/rs78529941"}]}