{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/NFIA","ko":"https://www.mygenelog.com/ko/api/v1/genes/NFIA"},"condition_count":13,"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":"NFIA","url":"https://www.mygenelog.com/ko/genes/NFIA","variant_count":39,"variants":[{"risk_tier":"sensitive","rsid":"rs1064794841","trait_name":"Chromosome 1p32-p31 deletion syndrome","url":"https://www.mygenelog.com/ko/variants/rs1064794841"},{"risk_tier":"standard","rsid":"rs12034786","trait_name":"Heel bone mineral density","url":"https://www.mygenelog.com/ko/variants/rs12034786"},{"risk_tier":"standard","rsid":"rs12134760","trait_name":"Educational attainment","url":"https://www.mygenelog.com/ko/variants/rs12134760"},{"risk_tier":"standard","rsid":"rs1255356768","trait_name":"Brain malformations with or without urinary tract defects","url":"https://www.mygenelog.com/ko/variants/rs1255356768"},{"risk_tier":"standard","rsid":"rs1422656895","trait_name":"Brain malformations with or without urinary tract defects","url":"https://www.mygenelog.com/ko/variants/rs1422656895"},{"risk_tier":"standard","rsid":"rs145711686","trait_name":"Free Cholesterol to Cholesteryl Esters in Small HDL ratio","url":"https://www.mygenelog.com/ko/variants/rs145711686"},{"risk_tier":"sensitive","rsid":"rs1553149182","trait_name":"NFIA-Related Disorder","url":"https://www.mygenelog.com/ko/variants/rs1553149182"},{"risk_tier":"standard","rsid":"rs1553149185","trait_name":"Brain malformations with or without urinary tract defects","url":"https://www.mygenelog.com/ko/variants/rs1553149185"},{"risk_tier":"sensitive","rsid":"rs1553182933","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1553182933"},{"risk_tier":"sensitive","rsid":"rs1570123287","trait_name":"Chromosome 1p32-p31 deletion syndrome","url":"https://www.mygenelog.com/ko/variants/rs1570123287"},{"risk_tier":"sensitive","rsid":"rs1646253231","trait_name":"Chromosome 1p32-p31 deletion syndrome","url":"https://www.mygenelog.com/ko/variants/rs1646253231"},{"risk_tier":"standard","rsid":"rs17121650","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs17121650"},{"risk_tier":"standard","rsid":"rs17121798","trait_name":"Low density lipoprotein cholesterol levels","url":"https://www.mygenelog.com/ko/variants/rs17121798"},{"risk_tier":"standard","rsid":"rs17265852","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs17265852"},{"risk_tier":"standard","rsid":"rs17375290","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs17375290"},{"risk_tier":"standard","rsid":"rs188503412","trait_name":"Triglyceride levels","url":"https://www.mygenelog.com/ko/variants/rs188503412"},{"risk_tier":"sensitive","rsid":"rs2100414767","trait_name":"Chromosome 1p32-p31 deletion syndrome","url":"https://www.mygenelog.com/ko/variants/rs2100414767"},{"risk_tier":"standard","rsid":"rs2207791","trait_name":"QRS duration","url":"https://www.mygenelog.com/ko/variants/rs2207791"},{"risk_tier":"standard","rsid":"rs2207793","trait_name":"Global electrical heterogeneity phenotypes","url":"https://www.mygenelog.com/ko/variants/rs2207793"},{"risk_tier":"standard","rsid":"rs2261787","trait_name":"Heart failure with reduced ejection fraction","url":"https://www.mygenelog.com/ko/variants/rs2261787"},{"risk_tier":"standard","rsid":"rs2474370","trait_name":"Heart failure","url":"https://www.mygenelog.com/ko/variants/rs2474370"},{"risk_tier":"standard","rsid":"rs2524179794","trait_name":"Brain malformations with or without urinary tract defects","url":"https://www.mygenelog.com/ko/variants/rs2524179794"},{"risk_tier":"standard","rsid":"rs310174","trait_name":"Primary open angle glaucoma (multi-trait analysis)","url":"https://www.mygenelog.com/ko/variants/rs310174"},{"risk_tier":"standard","rsid":"rs332827","trait_name":"Externalizing behaviour (multivariate analysis)","url":"https://www.mygenelog.com/ko/variants/rs332827"},{"risk_tier":"standard","rsid":"rs333166","trait_name":"Cystatin C levels","url":"https://www.mygenelog.com/ko/variants/rs333166"},{"risk_tier":"sensitive","rsid":"rs334701","trait_name":"Thyroid cancer","url":"https://www.mygenelog.com/ko/variants/rs334701"},{"risk_tier":"standard","rsid":"rs479445","trait_name":"Myopia (age of diagnosis)","url":"https://www.mygenelog.com/ko/variants/rs479445"},{"risk_tier":"standard","rsid":"rs59708846","trait_name":"Sex hormone-binding globulin levels adjusted for BMI","url":"https://www.mygenelog.com/ko/variants/rs59708846"},{"risk_tier":"standard","rsid":"rs6587924","trait_name":"Myocardial fractal dimension (slice 6)","url":"https://www.mygenelog.com/ko/variants/rs6587924"},{"risk_tier":"standard","rsid":"rs6693597","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs6693597"},{"risk_tier":"standard","rsid":"rs74090351","trait_name":"Sex hormone-binding globulin levels","url":"https://www.mygenelog.com/ko/variants/rs74090351"},{"risk_tier":"standard","rsid":"rs74328314","trait_name":"Phospholipids in large VLDL","url":"https://www.mygenelog.com/ko/variants/rs74328314"},{"risk_tier":"standard","rsid":"rs75481391","trait_name":"Triglyceride levels","url":"https://www.mygenelog.com/ko/variants/rs75481391"},{"risk_tier":"standard","rsid":"rs76776318","trait_name":"Red blood cell count","url":"https://www.mygenelog.com/ko/variants/rs76776318"},{"risk_tier":"sensitive","rsid":"rs769522583","trait_name":"Chromosome 1p32-p31 deletion syndrome","url":"https://www.mygenelog.com/ko/variants/rs769522583"},{"risk_tier":"standard","rsid":"rs868110","trait_name":"Triglycerides","url":"https://www.mygenelog.com/ko/variants/rs868110"},{"risk_tier":"standard","rsid":"rs876214","trait_name":"Spherical equivalent","url":"https://www.mygenelog.com/ko/variants/rs876214"},{"risk_tier":"sensitive","rsid":"rs9436635","trait_name":"Osteoarthritis (hip)","url":"https://www.mygenelog.com/ko/variants/rs9436635"},{"risk_tier":"standard","rsid":"rs9970140","trait_name":"Cholesteryl Esters to Total Lipids in Very Small VLDL percentage","url":"https://www.mygenelog.com/ko/variants/rs9970140"}]}