{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/MTOR","ko":"https://www.mygenelog.com/ko/api/v1/genes/MTOR"},"condition_count":7,"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":"MTOR","url":"https://www.mygenelog.com/genes/MTOR","variant_count":37,"variants":[{"risk_tier":"sensitive","rsid":"rs1010447","trait_name":"Body mass index and type 2 diabetes (pairwise)","url":"https://www.mygenelog.com/variants/rs1010447"},{"risk_tier":"standard","rsid":"rs1034528","trait_name":"Alanine aminotransferase levels","url":"https://www.mygenelog.com/variants/rs1034528"},{"risk_tier":"standard","rsid":"rs1057519779","trait_name":"Isolated focal cortical dysplasia type II","url":"https://www.mygenelog.com/variants/rs1057519779"},{"risk_tier":"standard","rsid":"rs1057519914","trait_name":"Hemimegalencephaly","url":"https://www.mygenelog.com/variants/rs1057519914"},{"risk_tier":"sensitive","rsid":"rs1057519915","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs1057519915"},{"risk_tier":"sensitive","rsid":"rs1057524044","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs1057524044"},{"risk_tier":"standard","rsid":"rs1085307113","trait_name":"Isolated focal cortical dysplasia type II","url":"https://www.mygenelog.com/variants/rs1085307113"},{"risk_tier":"standard","rsid":"rs113155158","trait_name":"Smoking initiation","url":"https://www.mygenelog.com/variants/rs113155158"},{"risk_tier":"standard","rsid":"rs1148480","trait_name":"height (mean, inv-normal transformed)","url":"https://www.mygenelog.com/variants/rs1148480"},{"risk_tier":"standard","rsid":"rs11581010","trait_name":"Body mass index","url":"https://www.mygenelog.com/variants/rs11581010"},{"risk_tier":"standard","rsid":"rs12089366","trait_name":"Body mass index","url":"https://www.mygenelog.com/variants/rs12089366"},{"risk_tier":"standard","rsid":"rs145166077","trait_name":"ANGPTL7 protein levels","url":"https://www.mygenelog.com/variants/rs145166077"},{"risk_tier":"standard","rsid":"rs147660927","trait_name":"Glaucoma (primary open-angle)","url":"https://www.mygenelog.com/variants/rs147660927"},{"risk_tier":"sensitive","rsid":"rs1553171141","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1553171141"},{"risk_tier":"standard","rsid":"rs1557739557","trait_name":"Macrocephaly","url":"https://www.mygenelog.com/variants/rs1557739557"},{"risk_tier":"standard","rsid":"rs187540244","trait_name":"Telomere length (principal component 1)","url":"https://www.mygenelog.com/variants/rs187540244"},{"risk_tier":"standard","rsid":"rs193140797","trait_name":"Kidney-associated antigen 1 levels","url":"https://www.mygenelog.com/variants/rs193140797"},{"risk_tier":"standard","rsid":"rs2076655","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs2076655"},{"risk_tier":"sensitive","rsid":"rs2100396600","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs2100396600"},{"risk_tier":"sensitive","rsid":"rs2100402606","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs2100402606"},{"risk_tier":"sensitive","rsid":"rs2100414567","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs2100414567"},{"risk_tier":"sensitive","rsid":"rs2100477650","trait_name":"Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes","url":"https://www.mygenelog.com/variants/rs2100477650"},{"risk_tier":"sensitive","rsid":"rs2100566800","trait_name":"Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes","url":"https://www.mygenelog.com/variants/rs2100566800"},{"risk_tier":"standard","rsid":"rs2100609915","trait_name":"Isolated focal cortical dysplasia type II","url":"https://www.mygenelog.com/variants/rs2100609915"},{"risk_tier":"standard","rsid":"rs2261434","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs2261434"},{"risk_tier":"standard","rsid":"rs56803472","trait_name":"Angiopoietin-related protein 7 levels","url":"https://www.mygenelog.com/variants/rs56803472"},{"risk_tier":"sensitive","rsid":"rs587777893","trait_name":"Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes","url":"https://www.mygenelog.com/variants/rs587777893"},{"risk_tier":"standard","rsid":"rs587777894","trait_name":"Isolated focal cortical dysplasia type II","url":"https://www.mygenelog.com/variants/rs587777894"},{"risk_tier":"sensitive","rsid":"rs587777900","trait_name":"CEBALID syndrome","url":"https://www.mygenelog.com/variants/rs587777900"},{"risk_tier":"standard","rsid":"rs6674994","trait_name":"Body shape phenotype PC2","url":"https://www.mygenelog.com/variants/rs6674994"},{"risk_tier":"sensitive","rsid":"rs6697896","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs6697896"},{"risk_tier":"standard","rsid":"rs77270747","trait_name":"Weight","url":"https://www.mygenelog.com/variants/rs77270747"},{"risk_tier":"sensitive","rsid":"rs786205165","trait_name":"CEBALID syndrome","url":"https://www.mygenelog.com/variants/rs786205165"},{"risk_tier":"sensitive","rsid":"rs863225264","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs863225264"},{"risk_tier":"sensitive","rsid":"rs869312666","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs869312666"},{"risk_tier":"sensitive","rsid":"rs869312671","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs869312671"},{"risk_tier":"sensitive","rsid":"rs878855328","trait_name":"Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome","url":"https://www.mygenelog.com/variants/rs878855328"}]}