{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/SHANK3","ko":"https://www.mygenelog.com/ko/api/v1/genes/SHANK3"},"condition_count":5,"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":"SHANK3","url":"https://www.mygenelog.com/genes/SHANK3","variant_count":29,"variants":[{"risk_tier":"sensitive","rsid":"rs1001153999","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs1001153999"},{"risk_tier":"sensitive","rsid":"rs1038102194","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs1038102194"},{"risk_tier":"sensitive","rsid":"rs1064795759","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs1064795759"},{"risk_tier":"standard","rsid":"rs1294272918","trait_name":"Autistic behavior","url":"https://www.mygenelog.com/variants/rs1294272918"},{"risk_tier":"sensitive","rsid":"rs1396379503","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs1396379503"},{"risk_tier":"standard","rsid":"rs1569097392","trait_name":"Global developmental delay","url":"https://www.mygenelog.com/variants/rs1569097392"},{"risk_tier":"sensitive","rsid":"rs1603447380","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs1603447380"},{"risk_tier":"sensitive","rsid":"rs1603447383","trait_name":"SHANK3-related disorder","url":"https://www.mygenelog.com/variants/rs1603447383"},{"risk_tier":"sensitive","rsid":"rs2083360139","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2083360139"},{"risk_tier":"sensitive","rsid":"rs2083361357","trait_name":"SHANK3-related disorder","url":"https://www.mygenelog.com/variants/rs2083361357"},{"risk_tier":"sensitive","rsid":"rs2146794652","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2146794652"},{"risk_tier":"sensitive","rsid":"rs2146833747","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2146833747"},{"risk_tier":"sensitive","rsid":"rs2518371253","trait_name":"SHANK3-related disorder","url":"https://www.mygenelog.com/variants/rs2518371253"},{"risk_tier":"sensitive","rsid":"rs2518393305","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2518393305"},{"risk_tier":"sensitive","rsid":"rs2518425257","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2518425257"},{"risk_tier":"sensitive","rsid":"rs2518429961","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2518429961"},{"risk_tier":"sensitive","rsid":"rs2518438901","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2518438901"},{"risk_tier":"sensitive","rsid":"rs2518439090","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs2518439090"},{"risk_tier":"sensitive","rsid":"rs373588048","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs373588048"},{"risk_tier":"sensitive","rsid":"rs387906932","trait_name":"Schizophrenia 15","url":"https://www.mygenelog.com/variants/rs387906932"},{"risk_tier":"sensitive","rsid":"rs387906933","trait_name":"Schizophrenia 15","url":"https://www.mygenelog.com/variants/rs387906933"},{"risk_tier":"sensitive","rsid":"rs397514705","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs397514705"},{"risk_tier":"standard","rsid":"rs541130164","trait_name":"Immunoglobulin M levels","url":"https://www.mygenelog.com/variants/rs541130164"},{"risk_tier":"standard","rsid":"rs5770820","trait_name":"Intelligence (MTAG)","url":"https://www.mygenelog.com/variants/rs5770820"},{"risk_tier":"standard","rsid":"rs6010042","trait_name":"Blood protein levels","url":"https://www.mygenelog.com/variants/rs6010042"},{"risk_tier":"standard","rsid":"rs6010044","trait_name":"Fibrinogen","url":"https://www.mygenelog.com/variants/rs6010044"},{"risk_tier":"standard","rsid":"rs7286601","trait_name":"Educational attainment (years of education)","url":"https://www.mygenelog.com/variants/rs7286601"},{"risk_tier":"sensitive","rsid":"rs763158627","trait_name":"Phelan-McDermid syndrome","url":"https://www.mygenelog.com/variants/rs763158627"},{"risk_tier":"standard","rsid":"rs8138473","trait_name":"Cognitive performance (MTAG)","url":"https://www.mygenelog.com/variants/rs8138473"}]}