{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/CLTC","ko":"https://www.mygenelog.com/ko/api/v1/genes/CLTC"},"condition_count":1,"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":"CLTC","url":"https://www.mygenelog.com/genes/CLTC","variant_count":26,"variants":[{"risk_tier":"standard","rsid":"rs1185165677","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs1185165677"},{"risk_tier":"standard","rsid":"rs1336573328","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs1336573328"},{"risk_tier":"standard","rsid":"rs142977590","trait_name":"GLIPR1 protein levels","url":"https://www.mygenelog.com/variants/rs142977590"},{"risk_tier":"sensitive","rsid":"rs1555605688","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1555605688"},{"risk_tier":"standard","rsid":"rs1555606635","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs1555606635"},{"risk_tier":"standard","rsid":"rs1555607159","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs1555607159"},{"risk_tier":"sensitive","rsid":"rs1555607504","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1555607504"},{"risk_tier":"standard","rsid":"rs1555607682","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs1555607682"},{"risk_tier":"standard","rsid":"rs1598211790","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs1598211790"},{"risk_tier":"standard","rsid":"rs17580385","trait_name":"Pulse pressure","url":"https://www.mygenelog.com/variants/rs17580385"},{"risk_tier":"sensitive","rsid":"rs2032737194","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2032737194"},{"risk_tier":"standard","rsid":"rs2143556646","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2143556646"},{"risk_tier":"standard","rsid":"rs2143591718","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2143591718"},{"risk_tier":"standard","rsid":"rs2143594831","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2143594831"},{"risk_tier":"standard","rsid":"rs2143602393","trait_name":"Abnormal corpus callosum morphology","url":"https://www.mygenelog.com/variants/rs2143602393"},{"risk_tier":"standard","rsid":"rs2509151066","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509151066"},{"risk_tier":"standard","rsid":"rs2509152675","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509152675"},{"risk_tier":"standard","rsid":"rs2509153854","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509153854"},{"risk_tier":"sensitive","rsid":"rs2509158550","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2509158550"},{"risk_tier":"standard","rsid":"rs2509357386","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509357386"},{"risk_tier":"sensitive","rsid":"rs2509361452","trait_name":"CLTC-related disorder","url":"https://www.mygenelog.com/variants/rs2509361452"},{"risk_tier":"standard","rsid":"rs2509384180","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509384180"},{"risk_tier":"standard","rsid":"rs2509384283","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509384283"},{"risk_tier":"standard","rsid":"rs2509384644","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs2509384644"},{"risk_tier":"standard","rsid":"rs367867382","trait_name":"Intellectual disability, autosomal dominant 56","url":"https://www.mygenelog.com/variants/rs367867382"},{"risk_tier":"sensitive","rsid":"rs781677731","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs781677731"}]}