{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/GNAI1","ko":"https://www.mygenelog.com/ko/api/v1/genes/GNAI1"},"condition_count":6,"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":"GNAI1","url":"https://www.mygenelog.com/ko/genes/GNAI1","variant_count":18,"variants":[{"risk_tier":"standard","rsid":"rs10241877","trait_name":"Triglycerides to Total Lipids in Large HDL percentage","url":"https://www.mygenelog.com/ko/variants/rs10241877"},{"risk_tier":"standard","rsid":"rs147399128","trait_name":"Free Cholesterol to Cholesteryl Esters in Large HDL ratio","url":"https://www.mygenelog.com/ko/variants/rs147399128"},{"risk_tier":"standard","rsid":"rs1788434297","trait_name":"Seizure","url":"https://www.mygenelog.com/ko/variants/rs1788434297"},{"risk_tier":"sensitive","rsid":"rs1788434338","trait_name":"Neurodevelopmental disorder","url":"https://www.mygenelog.com/ko/variants/rs1788434338"},{"risk_tier":"sensitive","rsid":"rs1788434582","trait_name":"GNAI1-related disorder","url":"https://www.mygenelog.com/ko/variants/rs1788434582"},{"risk_tier":"sensitive","rsid":"rs1788863320","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs1788863320"},{"risk_tier":"sensitive","rsid":"rs1788864590","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs1788864590"},{"risk_tier":"sensitive","rsid":"rs2115631937","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2115631937"},{"risk_tier":"sensitive","rsid":"rs2115683966","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2115683966"},{"risk_tier":"sensitive","rsid":"rs2115712676","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2115712676"},{"risk_tier":"sensitive","rsid":"rs2115712706","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2115712706"},{"risk_tier":"sensitive","rsid":"rs2115712712","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2115712712"},{"risk_tier":"sensitive","rsid":"rs2115727431","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2115727431"},{"risk_tier":"sensitive","rsid":"rs2116052322","trait_name":"Neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities","url":"https://www.mygenelog.com/ko/variants/rs2116052322"},{"risk_tier":"standard","rsid":"rs571552226","trait_name":"Malignant neoplasm of renal pelvis (PheCode 189.12)","url":"https://www.mygenelog.com/ko/variants/rs571552226"},{"risk_tier":"standard","rsid":"rs76728446","trait_name":"Triglycerides to Total Lipids in Medium HDL percentage","url":"https://www.mygenelog.com/ko/variants/rs76728446"},{"risk_tier":"standard","rsid":"rs799979","trait_name":"Cognitive decline rate in late mild cognitive impairment","url":"https://www.mygenelog.com/ko/variants/rs799979"},{"risk_tier":"standard","rsid":"rs9640815","trait_name":"Educational attainment","url":"https://www.mygenelog.com/ko/variants/rs9640815"}]}