{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/FBXW7","ko":"https://www.mygenelog.com/ko/api/v1/genes/FBXW7"},"condition_count":6,"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":"FBXW7","url":"https://www.mygenelog.com/genes/FBXW7","variant_count":19,"variants":[{"risk_tier":"standard","rsid":"rs11931711","trait_name":"Eosinophil count","url":"https://www.mygenelog.com/variants/rs11931711"},{"risk_tier":"standard","rsid":"rs140856583","trait_name":"Developmental delay, hypotonia, and impaired language","url":"https://www.mygenelog.com/variants/rs140856583"},{"risk_tier":"sensitive","rsid":"rs149680468","trait_name":"FBXW7-related neurodevelopmental disorder","url":"https://www.mygenelog.com/variants/rs149680468"},{"risk_tier":"standard","rsid":"rs17277029","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs17277029"},{"risk_tier":"standard","rsid":"rs202044741","trait_name":"Height (baseline)","url":"https://www.mygenelog.com/variants/rs202044741"},{"risk_tier":"standard","rsid":"rs2126459625","trait_name":"Developmental delay, hypotonia, and impaired language","url":"https://www.mygenelog.com/variants/rs2126459625"},{"risk_tier":"sensitive","rsid":"rs2126464225","trait_name":"Neurodevelopmental disorder","url":"https://www.mygenelog.com/variants/rs2126464225"},{"risk_tier":"sensitive","rsid":"rs2126466009","trait_name":"Neurodevelopmental disorder","url":"https://www.mygenelog.com/variants/rs2126466009"},{"risk_tier":"sensitive","rsid":"rs2126475180","trait_name":"FBXW7-related disorder","url":"https://www.mygenelog.com/variants/rs2126475180"},{"risk_tier":"sensitive","rsid":"rs2126476768","trait_name":"FBXW7-related disorder","url":"https://www.mygenelog.com/variants/rs2126476768"},{"risk_tier":"standard","rsid":"rs2126497313","trait_name":"Developmental delay, hypotonia, and impaired language","url":"https://www.mygenelog.com/variants/rs2126497313"},{"risk_tier":"sensitive","rsid":"rs2126497487","trait_name":"Inborn genetic diseases","url":"https://www.mygenelog.com/variants/rs2126497487"},{"risk_tier":"standard","rsid":"rs2126515961","trait_name":"Developmental delay, hypotonia, and impaired language","url":"https://www.mygenelog.com/variants/rs2126515961"},{"risk_tier":"standard","rsid":"rs2126525665","trait_name":"Medulloblastoma WNT activated","url":"https://www.mygenelog.com/variants/rs2126525665"},{"risk_tier":"sensitive","rsid":"rs2126583593","trait_name":"Neurodevelopmental disorder","url":"https://www.mygenelog.com/variants/rs2126583593"},{"risk_tier":"standard","rsid":"rs2530191471","trait_name":"Developmental delay, hypotonia, and impaired language","url":"https://www.mygenelog.com/variants/rs2530191471"},{"risk_tier":"standard","rsid":"rs6535847","trait_name":"Eosinophill count (UKB data field 30150)","url":"https://www.mygenelog.com/variants/rs6535847"},{"risk_tier":"sensitive","rsid":"rs66479472","trait_name":"Type 2 diabetes","url":"https://www.mygenelog.com/variants/rs66479472"},{"risk_tier":"sensitive","rsid":"rs867384286","trait_name":"Colorectal cancer","url":"https://www.mygenelog.com/variants/rs867384286"}]}