{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/PRUNE1","ko":"https://www.mygenelog.com/ko/api/v1/genes/PRUNE1"},"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":"PRUNE1","url":"https://www.mygenelog.com/genes/PRUNE1","variant_count":20,"variants":[{"risk_tier":"standard","rsid":"rs1057521927","trait_name":"Abnormal brain morphology","url":"https://www.mygenelog.com/variants/rs1057521927"},{"risk_tier":"sensitive","rsid":"rs1085308033","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs1085308033"},{"risk_tier":"standard","rsid":"rs11204763","trait_name":"CA14 protein levels","url":"https://www.mygenelog.com/variants/rs11204763"},{"risk_tier":"standard","rsid":"rs112822759","trait_name":"MINDY1 protein levels","url":"https://www.mygenelog.com/variants/rs112822759"},{"risk_tier":"standard","rsid":"rs12117525","trait_name":"Fasting blood glucose","url":"https://www.mygenelog.com/variants/rs12117525"},{"risk_tier":"sensitive","rsid":"rs1232331611","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs1232331611"},{"risk_tier":"sensitive","rsid":"rs137929776","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs137929776"},{"risk_tier":"sensitive","rsid":"rs1456845940","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs1456845940"},{"risk_tier":"sensitive","rsid":"rs1674200670","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs1674200670"},{"risk_tier":"standard","rsid":"rs200618384","trait_name":"Abnormal brain morphology","url":"https://www.mygenelog.com/variants/rs200618384"},{"risk_tier":"sensitive","rsid":"rs2528381693","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs2528381693"},{"risk_tier":"sensitive","rsid":"rs587684563","trait_name":"PRUNE1-related disorder","url":"https://www.mygenelog.com/variants/rs587684563"},{"risk_tier":"standard","rsid":"rs6661135","trait_name":"Trauma exposure","url":"https://www.mygenelog.com/variants/rs6661135"},{"risk_tier":"standard","rsid":"rs6673178","trait_name":"CDSN protein levels","url":"https://www.mygenelog.com/variants/rs6673178"},{"risk_tier":"standard","rsid":"rs6684154","trait_name":"Liver enzyme levels (alanine transaminase)","url":"https://www.mygenelog.com/variants/rs6684154"},{"risk_tier":"sensitive","rsid":"rs752599948","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs752599948"},{"risk_tier":"standard","rsid":"rs76104463","trait_name":"CA14 protein levels","url":"https://www.mygenelog.com/variants/rs76104463"},{"risk_tier":"standard","rsid":"rs767769359","trait_name":"Abnormal brain morphology","url":"https://www.mygenelog.com/variants/rs767769359"},{"risk_tier":"standard","rsid":"rs773618224","trait_name":"Abnormal brain morphology","url":"https://www.mygenelog.com/variants/rs773618224"},{"risk_tier":"sensitive","rsid":"rs886039608","trait_name":"Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","url":"https://www.mygenelog.com/variants/rs886039608"}]}