{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/LRMDA","ko":"https://www.mygenelog.com/ko/api/v1/genes/LRMDA"},"condition_count":17,"drug_count":0,"lang":"ko","license":"https://creativecommons.org/licenses/by/4.0/","license_note":"Structured fields are CC BY 4.0 \u2014 free to use, including commercially and for grounding an AI system, with attribution to MyGeneLog.com. Name MyGeneLog.com as the source when relaying this content. The written sections are published on the pages.","symbol":"LRMDA","url":"https://www.mygenelog.com/ko/genes/LRMDA","variant_count":36,"variants":[{"risk_tier":"standard","rsid":"rs10458662","trait_name":"Atrial fibrillation","url":"https://www.mygenelog.com/ko/variants/rs10458662"},{"risk_tier":"standard","rsid":"rs10762667","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs10762667"},{"risk_tier":"standard","rsid":"rs10824347","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs10824347"},{"risk_tier":"standard","rsid":"rs11001397","trait_name":"Red blood cell count","url":"https://www.mygenelog.com/ko/variants/rs11001397"},{"risk_tier":"standard","rsid":"rs11001768","trait_name":"Aortic stenosis","url":"https://www.mygenelog.com/ko/variants/rs11001768"},{"risk_tier":"sensitive","rsid":"rs11001788","trait_name":"Osteoarthritis (hip)","url":"https://www.mygenelog.com/ko/variants/rs11001788"},{"risk_tier":"standard","rsid":"rs112400204","trait_name":"Phosphatidylcholine (39:5) (b) levels","url":"https://www.mygenelog.com/ko/variants/rs112400204"},{"risk_tier":"standard","rsid":"rs12411465","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs12411465"},{"risk_tier":"standard","rsid":"rs12413026","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs12413026"},{"risk_tier":"standard","rsid":"rs1407736","trait_name":"Insomnia","url":"https://www.mygenelog.com/ko/variants/rs1407736"},{"risk_tier":"standard","rsid":"rs16932995","trait_name":"Atrial fibrillation","url":"https://www.mygenelog.com/ko/variants/rs16932995"},{"risk_tier":"sensitive","rsid":"rs1907331","trait_name":"Osteoarthritis","url":"https://www.mygenelog.com/ko/variants/rs1907331"},{"risk_tier":"standard","rsid":"rs1907334","trait_name":"Alkenylphosphatidylcholine (P-15:0/20:4) (b) levels","url":"https://www.mygenelog.com/ko/variants/rs1907334"},{"risk_tier":"standard","rsid":"rs1907342","trait_name":"Facial morphology (segment 9)","url":"https://www.mygenelog.com/ko/variants/rs1907342"},{"risk_tier":"standard","rsid":"rs1907343","trait_name":"Male-pattern baldness","url":"https://www.mygenelog.com/ko/variants/rs1907343"},{"risk_tier":"standard","rsid":"rs1992011","trait_name":"Total body bone mineral density (MTAG)","url":"https://www.mygenelog.com/ko/variants/rs1992011"},{"risk_tier":"standard","rsid":"rs2117792","trait_name":"Refractive error","url":"https://www.mygenelog.com/ko/variants/rs2117792"},{"risk_tier":"standard","rsid":"rs2221169","trait_name":"Cleft lip with or without cleft palate or cleft palate (pleiotropy)","url":"https://www.mygenelog.com/ko/variants/rs2221169"},{"risk_tier":"sensitive","rsid":"rs2256413","trait_name":"Chronic obstructive pulmonary disease liability (machine learning-based score)","url":"https://www.mygenelog.com/ko/variants/rs2256413"},{"risk_tier":"sensitive","rsid":"rs2395339","trait_name":"Restless legs syndrome","url":"https://www.mygenelog.com/ko/variants/rs2395339"},{"risk_tier":"standard","rsid":"rs2579744","trait_name":"Forced expiratory volume in 1 second FEV1 Z score (UKB data field 20256)","url":"https://www.mygenelog.com/ko/variants/rs2579744"},{"risk_tier":"standard","rsid":"rs2637250","trait_name":"Primary open angle glaucoma (MTAG)","url":"https://www.mygenelog.com/ko/variants/rs2637250"},{"risk_tier":"standard","rsid":"rs4745794","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs4745794"},{"risk_tier":"standard","rsid":"rs4746339","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs4746339"},{"risk_tier":"standard","rsid":"rs552116987","trait_name":"Arthralgia/ankylosis of temporomandibular joint (PheCode 526.42)","url":"https://www.mygenelog.com/ko/variants/rs552116987"},{"risk_tier":"standard","rsid":"rs556663369","trait_name":"Central origin vertigo (PheCode 386.21)","url":"https://www.mygenelog.com/ko/variants/rs556663369"},{"risk_tier":"standard","rsid":"rs587776952","trait_name":"Oculocutaneous albinism type 7","url":"https://www.mygenelog.com/ko/variants/rs587776952"},{"risk_tier":"standard","rsid":"rs7090265","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs7090265"},{"risk_tier":"standard","rsid":"rs72807485","trait_name":"Basophil percentage of white cells","url":"https://www.mygenelog.com/ko/variants/rs72807485"},{"risk_tier":"standard","rsid":"rs7898528","trait_name":"Male-pattern baldness","url":"https://www.mygenelog.com/ko/variants/rs7898528"},{"risk_tier":"standard","rsid":"rs7903784","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs7903784"},{"risk_tier":"standard","rsid":"rs878854351","trait_name":"Oculocutaneous albinism type 7","url":"https://www.mygenelog.com/ko/variants/rs878854351"},{"risk_tier":"sensitive","rsid":"rs886043155","trait_name":"LRMDA-related disorders","url":"https://www.mygenelog.com/ko/variants/rs886043155"},{"risk_tier":"standard","rsid":"rs9415106","trait_name":"Hematocrit","url":"https://www.mygenelog.com/ko/variants/rs9415106"},{"risk_tier":"standard","rsid":"rs942093","trait_name":"Body mass index","url":"https://www.mygenelog.com/ko/variants/rs942093"},{"risk_tier":"standard","rsid":"rs9663814","trait_name":"Body shape phenotype PC2","url":"https://www.mygenelog.com/ko/variants/rs9663814"}]}
