{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/PI4KA","ko":"https://www.mygenelog.com/ko/api/v1/genes/PI4KA"},"condition_count":2,"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":"PI4KA","url":"https://www.mygenelog.com/genes/PI4KA","variant_count":24,"variants":[{"risk_tier":"sensitive","rsid":"rs116401176","trait_name":"O-acetyl-ADP-ribose deacetylase MACROD2 level in Chronic kidney disease with hypertension and no diabetes (25459_3)","url":"https://www.mygenelog.com/variants/rs116401176"},{"risk_tier":"standard","rsid":"rs116900838","trait_name":"Mean platelet volume during second trimester of pregnancy","url":"https://www.mygenelog.com/variants/rs116900838"},{"risk_tier":"standard","rsid":"rs117077073","trait_name":"Mean platelet volume during third trimester of pregnancy","url":"https://www.mygenelog.com/variants/rs117077073"},{"risk_tier":"standard","rsid":"rs117357866","trait_name":"Platelet count","url":"https://www.mygenelog.com/variants/rs117357866"},{"risk_tier":"sensitive","rsid":"rs1202099178","trait_name":"PI4KA-related disorder","url":"https://www.mygenelog.com/variants/rs1202099178"},{"risk_tier":"standard","rsid":"rs1351749039","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs1351749039"},{"risk_tier":"standard","rsid":"rs146132285","trait_name":"Mean platelet volume","url":"https://www.mygenelog.com/variants/rs146132285"},{"risk_tier":"standard","rsid":"rs1490645147","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs1490645147"},{"risk_tier":"standard","rsid":"rs165818","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs165818"},{"risk_tier":"standard","rsid":"rs190123700","trait_name":"Platelet count","url":"https://www.mygenelog.com/variants/rs190123700"},{"risk_tier":"standard","rsid":"rs1929601378","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs1929601378"},{"risk_tier":"standard","rsid":"rs201395198","trait_name":"Spastic paraplegia 84, autosomal recessive","url":"https://www.mygenelog.com/variants/rs201395198"},{"risk_tier":"standard","rsid":"rs2147164417","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs2147164417"},{"risk_tier":"standard","rsid":"rs2147171210","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs2147171210"},{"risk_tier":"standard","rsid":"rs2147194890","trait_name":"Spastic paraplegia 84, autosomal recessive","url":"https://www.mygenelog.com/variants/rs2147194890"},{"risk_tier":"standard","rsid":"rs2147287553","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs2147287553"},{"risk_tier":"standard","rsid":"rs28754290","trait_name":"Monocyte percentage of white cells","url":"https://www.mygenelog.com/variants/rs28754290"},{"risk_tier":"standard","rsid":"rs6004122","trait_name":"Leucine-rich repeat serine/threonine-protein kinase 2 levels","url":"https://www.mygenelog.com/variants/rs6004122"},{"risk_tier":"standard","rsid":"rs747119727","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs747119727"},{"risk_tier":"sensitive","rsid":"rs762036318","trait_name":"PI4KA-related disorder","url":"https://www.mygenelog.com/variants/rs762036318"},{"risk_tier":"standard","rsid":"rs767451281","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs767451281"},{"risk_tier":"standard","rsid":"rs775166339","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs775166339"},{"risk_tier":"sensitive","rsid":"rs776650691","trait_name":"Gastrointestinal defects and immunodeficiency syndrome 2","url":"https://www.mygenelog.com/variants/rs776650691"},{"risk_tier":"standard","rsid":"rs777006911","trait_name":"Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","url":"https://www.mygenelog.com/variants/rs777006911"}]}