{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/GP1BA","ko":"https://www.mygenelog.com/ko/api/v1/genes/GP1BA"},"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":"GP1BA","url":"https://www.mygenelog.com/genes/GP1BA","variant_count":25,"variants":[{"risk_tier":"sensitive","rsid":"rs121908061","trait_name":"Bernard-Soulier syndrome, type A1","url":"https://www.mygenelog.com/variants/rs121908061"},{"risk_tier":"sensitive","rsid":"rs121908062","trait_name":"Pseudo von Willebrand disease","url":"https://www.mygenelog.com/variants/rs121908062"},{"risk_tier":"sensitive","rsid":"rs121908063","trait_name":"Bernard-Soulier syndrome, type A2, autosomal dominant","url":"https://www.mygenelog.com/variants/rs121908063"},{"risk_tier":"sensitive","rsid":"rs121908064","trait_name":"Pseudo von Willebrand disease","url":"https://www.mygenelog.com/variants/rs121908064"},{"risk_tier":"sensitive","rsid":"rs121908065","trait_name":"Bernard-Soulier syndrome, type A1","url":"https://www.mygenelog.com/variants/rs121908065"},{"risk_tier":"sensitive","rsid":"rs1394634674","trait_name":"Bernard-Soulier syndrome, type A1","url":"https://www.mygenelog.com/variants/rs1394634674"},{"risk_tier":"sensitive","rsid":"rs1597638300","trait_name":"Bernard-Soulier syndrome, type A2, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1597638300"},{"risk_tier":"sensitive","rsid":"rs1597638598","trait_name":"Thrombocytopenia","url":"https://www.mygenelog.com/variants/rs1597638598"},{"risk_tier":"sensitive","rsid":"rs1597638745","trait_name":"Bernard-Soulier syndrome, type A2, autosomal dominant","url":"https://www.mygenelog.com/variants/rs1597638745"},{"risk_tier":"sensitive","rsid":"rs1597639057","trait_name":"Thrombocytopenia","url":"https://www.mygenelog.com/variants/rs1597639057"},{"risk_tier":"standard","rsid":"rs1970365829","trait_name":"Abnormal bleeding","url":"https://www.mygenelog.com/variants/rs1970365829"},{"risk_tier":"sensitive","rsid":"rs2151107661","trait_name":"Bernard-Soulier syndrome, type A2, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2151107661"},{"risk_tier":"sensitive","rsid":"rs2151107674","trait_name":"Bernard Soulier syndrome","url":"https://www.mygenelog.com/variants/rs2151107674"},{"risk_tier":"sensitive","rsid":"rs2151107705","trait_name":"Bernard-Soulier syndrome, type A2, autosomal dominant","url":"https://www.mygenelog.com/variants/rs2151107705"},{"risk_tier":"sensitive","rsid":"rs2151107940","trait_name":"Bernard Soulier syndrome","url":"https://www.mygenelog.com/variants/rs2151107940"},{"risk_tier":"sensitive","rsid":"rs2151107964","trait_name":"Pseudo von Willebrand disease","url":"https://www.mygenelog.com/variants/rs2151107964"},{"risk_tier":"sensitive","rsid":"rs2507593310","trait_name":"Bernard Soulier syndrome","url":"https://www.mygenelog.com/variants/rs2507593310"},{"risk_tier":"sensitive","rsid":"rs267606849","trait_name":"Bernard-Soulier syndrome, type A1","url":"https://www.mygenelog.com/variants/rs267606849"},{"risk_tier":"standard","rsid":"rs553749201","trait_name":"Mean platelet volume","url":"https://www.mygenelog.com/variants/rs553749201"},{"risk_tier":"standard","rsid":"rs56337033","trait_name":"Platelet distribution width","url":"https://www.mygenelog.com/variants/rs56337033"},{"risk_tier":"sensitive","rsid":"rs753768072","trait_name":"Bernard Soulier syndrome","url":"https://www.mygenelog.com/variants/rs753768072"},{"risk_tier":"sensitive","rsid":"rs765474118","trait_name":"Pseudo von Willebrand disease","url":"https://www.mygenelog.com/variants/rs765474118"},{"risk_tier":"sensitive","rsid":"rs767224320","trait_name":"Bernard-Soulier syndrome, type A2, autosomal dominant","url":"https://www.mygenelog.com/variants/rs767224320"},{"risk_tier":"sensitive","rsid":"rs771048666","trait_name":"Bernard Soulier syndrome","url":"https://www.mygenelog.com/variants/rs771048666"},{"risk_tier":"sensitive","rsid":"rs781541857","trait_name":"Bernard Soulier syndrome","url":"https://www.mygenelog.com/variants/rs781541857"}]}