{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/PPP1R21","ko":"https://www.mygenelog.com/ko/api/v1/genes/PPP1R21"},"condition_count":4,"drug_count":0,"lang":"ko","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":"PPP1R21","url":"https://www.mygenelog.com/ko/genes/PPP1R21","variant_count":12,"variants":[{"risk_tier":"standard","rsid":"rs11678825","trait_name":"Reticulocyte fraction of red cells","url":"https://www.mygenelog.com/ko/variants/rs11678825"},{"risk_tier":"standard","rsid":"rs12620002","trait_name":"Mean corpuscular hemoglobin concentration","url":"https://www.mygenelog.com/ko/variants/rs12620002"},{"risk_tier":"sensitive","rsid":"rs1667894875","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/ko/variants/rs1667894875"},{"risk_tier":"sensitive","rsid":"rs370271261","trait_name":"Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities","url":"https://www.mygenelog.com/ko/variants/rs370271261"},{"risk_tier":"standard","rsid":"rs61387839","trait_name":"Educational attainment (years of education)","url":"https://www.mygenelog.com/ko/variants/rs61387839"},{"risk_tier":"standard","rsid":"rs7566996","trait_name":"Height","url":"https://www.mygenelog.com/ko/variants/rs7566996"},{"risk_tier":"standard","rsid":"rs7575998","trait_name":"Reticulocyte percentage (UKB data field 30240)","url":"https://www.mygenelog.com/ko/variants/rs7575998"},{"risk_tier":"standard","rsid":"rs77272589","trait_name":"Red blood cell count","url":"https://www.mygenelog.com/ko/variants/rs77272589"},{"risk_tier":"standard","rsid":"rs78538011","trait_name":"Red blood cell count","url":"https://www.mygenelog.com/ko/variants/rs78538011"},{"risk_tier":"sensitive","rsid":"rs866802950","trait_name":"Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities","url":"https://www.mygenelog.com/ko/variants/rs866802950"},{"risk_tier":"sensitive","rsid":"rs989639063","trait_name":"Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities","url":"https://www.mygenelog.com/ko/variants/rs989639063"},{"risk_tier":"sensitive","rsid":"rs998498095","trait_name":"Neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities","url":"https://www.mygenelog.com/ko/variants/rs998498095"}]}