{"alternates":{"en":"https://www.mygenelog.com/api/v1/genes/FGFR2","ko":"https://www.mygenelog.com/ko/api/v1/genes/FGFR2"},"condition_count":9,"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":"FGFR2","url":"https://www.mygenelog.com/genes/FGFR2","variant_count":86,"variants":[{"risk_tier":"sensitive","rsid":"rs10510097","trait_name":"Breast cancer","url":"https://www.mygenelog.com/variants/rs10510097"},{"risk_tier":"sensitive","rsid":"rs1057519036","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519036"},{"risk_tier":"sensitive","rsid":"rs1057519038","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519038"},{"risk_tier":"sensitive","rsid":"rs1057519039","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519039"},{"risk_tier":"sensitive","rsid":"rs1057519040","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519040"},{"risk_tier":"standard","rsid":"rs1057519041","trait_name":"Acrocephalosyndactyly type I","url":"https://www.mygenelog.com/variants/rs1057519041"},{"risk_tier":"sensitive","rsid":"rs1057519042","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519042"},{"risk_tier":"sensitive","rsid":"rs1057519043","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519043"},{"risk_tier":"sensitive","rsid":"rs1057519044","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519044"},{"risk_tier":"sensitive","rsid":"rs1057519045","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs1057519045"},{"risk_tier":"sensitive","rsid":"rs1057519047","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs1057519047"},{"risk_tier":"standard","rsid":"rs10788160","trait_name":"Serum prostate-specific antigen levels","url":"https://www.mygenelog.com/variants/rs10788160"},{"risk_tier":"standard","rsid":"rs11592107","trait_name":"Systolic blood pressure","url":"https://www.mygenelog.com/variants/rs11592107"},{"risk_tier":"sensitive","rsid":"rs121913474","trait_name":"Beare-Stevenson cutis gyrata syndrome","url":"https://www.mygenelog.com/variants/rs121913474"},{"risk_tier":"sensitive","rsid":"rs121913477","trait_name":"Beare-Stevenson cutis gyrata syndrome","url":"https://www.mygenelog.com/variants/rs121913477"},{"risk_tier":"sensitive","rsid":"rs121913478","trait_name":"Beare-Stevenson cutis gyrata syndrome","url":"https://www.mygenelog.com/variants/rs121913478"},{"risk_tier":"sensitive","rsid":"rs121918487","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918487"},{"risk_tier":"sensitive","rsid":"rs121918488","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918488"},{"risk_tier":"sensitive","rsid":"rs121918489","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918489"},{"risk_tier":"sensitive","rsid":"rs121918490","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918490"},{"risk_tier":"sensitive","rsid":"rs121918491","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918491"},{"risk_tier":"sensitive","rsid":"rs121918492","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918492"},{"risk_tier":"sensitive","rsid":"rs121918493","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918493"},{"risk_tier":"sensitive","rsid":"rs121918494","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918494"},{"risk_tier":"sensitive","rsid":"rs121918495","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs121918495"},{"risk_tier":"sensitive","rsid":"rs121918496","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918496"},{"risk_tier":"sensitive","rsid":"rs121918497","trait_name":"Jackson-Weiss syndrome","url":"https://www.mygenelog.com/variants/rs121918497"},{"risk_tier":"sensitive","rsid":"rs121918499","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs121918499"},{"risk_tier":"sensitive","rsid":"rs121918500","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918500"},{"risk_tier":"sensitive","rsid":"rs121918501","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918501"},{"risk_tier":"sensitive","rsid":"rs121918502","trait_name":"Pfeiffer syndrome type 3","url":"https://www.mygenelog.com/variants/rs121918502"},{"risk_tier":"sensitive","rsid":"rs121918505","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs121918505"},{"risk_tier":"sensitive","rsid":"rs121918506","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs121918506"},{"risk_tier":"sensitive","rsid":"rs121918507","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs121918507"},{"risk_tier":"sensitive","rsid":"rs121918508","trait_name":"Levy-Hollister syndrome","url":"https://www.mygenelog.com/variants/rs121918508"},{"risk_tier":"sensitive","rsid":"rs121918509","trait_name":"LADD syndrome 1","url":"https://www.mygenelog.com/variants/rs121918509"},{"risk_tier":"sensitive","rsid":"rs121918510","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs121918510"},{"risk_tier":"standard","rsid":"rs1274989878","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1274989878"},{"risk_tier":"standard","rsid":"rs1358919643","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1358919643"},{"risk_tier":"standard","rsid":"rs138358320","trait_name":"Atrial fibrillation","url":"https://www.mygenelog.com/variants/rs138358320"},{"risk_tier":"standard","rsid":"rs1434545235","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1434545235"},{"risk_tier":"sensitive","rsid":"rs1554907337","trait_name":"Levy-Hollister syndrome","url":"https://www.mygenelog.com/variants/rs1554907337"},{"risk_tier":"sensitive","rsid":"rs1554917471","trait_name":"Levy-Hollister syndrome","url":"https://www.mygenelog.com/variants/rs1554917471"},{"risk_tier":"standard","rsid":"rs1554927408","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1554927408"},{"risk_tier":"standard","rsid":"rs1554928884","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1554928884"},{"risk_tier":"standard","rsid":"rs1554930790","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1554930790"},{"risk_tier":"standard","rsid":"rs1564919048","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1564919048"},{"risk_tier":"standard","rsid":"rs1589722765","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1589722765"},{"risk_tier":"sensitive","rsid":"rs1649199","trait_name":"Dupuytren's disease","url":"https://www.mygenelog.com/variants/rs1649199"},{"risk_tier":"standard","rsid":"rs17541509","trait_name":"Vertex-wise sulcal depth","url":"https://www.mygenelog.com/variants/rs17541509"},{"risk_tier":"sensitive","rsid":"rs17542768","trait_name":"Breast cancer","url":"https://www.mygenelog.com/variants/rs17542768"},{"risk_tier":"standard","rsid":"rs1845559552","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1845559552"},{"risk_tier":"sensitive","rsid":"rs1847510893","trait_name":"Levy-Hollister syndrome","url":"https://www.mygenelog.com/variants/rs1847510893"},{"risk_tier":"standard","rsid":"rs1850289942","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs1850289942"},{"risk_tier":"standard","rsid":"rs2133823028","trait_name":"Bilateral sensorineural hearing impairment","url":"https://www.mygenelog.com/variants/rs2133823028"},{"risk_tier":"standard","rsid":"rs2133825396","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2133825396"},{"risk_tier":"standard","rsid":"rs2133835239","trait_name":"Acrocephalosyndactyly type I","url":"https://www.mygenelog.com/variants/rs2133835239"},{"risk_tier":"standard","rsid":"rs2133944245","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2133944245"},{"risk_tier":"sensitive","rsid":"rs2133975330","trait_name":"Levy-Hollister syndrome","url":"https://www.mygenelog.com/variants/rs2133975330"},{"risk_tier":"standard","rsid":"rs2134253566","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2134253566"},{"risk_tier":"standard","rsid":"rs2134253609","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2134253609"},{"risk_tier":"standard","rsid":"rs2134253669","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2134253669"},{"risk_tier":"standard","rsid":"rs2134254345","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2134254345"},{"risk_tier":"standard","rsid":"rs2134256250","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2134256250"},{"risk_tier":"standard","rsid":"rs2134260022","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2134260022"},{"risk_tier":"sensitive","rsid":"rs2539419195","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs2539419195"},{"risk_tier":"standard","rsid":"rs2540045968","trait_name":"FGFR2-related craniosynostosis","url":"https://www.mygenelog.com/variants/rs2540045968"},{"risk_tier":"sensitive","rsid":"rs2912780","trait_name":"Breast cancer","url":"https://www.mygenelog.com/variants/rs2912780"},{"risk_tier":"standard","rsid":"rs2981430","trait_name":"FGFR2 protein levels","url":"https://www.mygenelog.com/variants/rs2981430"},{"risk_tier":"standard","rsid":"rs2981453","trait_name":"Gamma glutamyl transferase levels","url":"https://www.mygenelog.com/variants/rs2981453"},{"risk_tier":"standard","rsid":"rs2981461","trait_name":"Creatinine levels","url":"https://www.mygenelog.com/variants/rs2981461"},{"risk_tier":"sensitive","rsid":"rs2981582","trait_name":"Breast cancer","url":"https://www.mygenelog.com/variants/rs2981582"},{"risk_tier":"standard","rsid":"rs3135715","trait_name":"Height","url":"https://www.mygenelog.com/variants/rs3135715"},{"risk_tier":"sensitive","rsid":"rs34032268","trait_name":"Prostate cancer","url":"https://www.mygenelog.com/variants/rs34032268"},{"risk_tier":"sensitive","rsid":"rs387906676","trait_name":"Crouzon syndrome","url":"https://www.mygenelog.com/variants/rs387906676"},{"risk_tier":"sensitive","rsid":"rs387906677","trait_name":"Bent bone dysplasia syndrome 1","url":"https://www.mygenelog.com/variants/rs387906677"},{"risk_tier":"sensitive","rsid":"rs387906678","trait_name":"Bent bone dysplasia syndrome 1","url":"https://www.mygenelog.com/variants/rs387906678"},{"risk_tier":"standard","rsid":"rs45631563","trait_name":"Prostate-specific antigen levels","url":"https://www.mygenelog.com/variants/rs45631563"},{"risk_tier":"sensitive","rsid":"rs45631632","trait_name":"Cancer (pleiotropy)","url":"https://www.mygenelog.com/variants/rs45631632"},{"risk_tier":"standard","rsid":"rs4751842","trait_name":"Prostate-specific antigen levels","url":"https://www.mygenelog.com/variants/rs4751842"},{"risk_tier":"standard","rsid":"rs77543610","trait_name":"Acrocephalosyndactyly type I","url":"https://www.mygenelog.com/variants/rs77543610"},{"risk_tier":"sensitive","rsid":"rs776587763","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs776587763"},{"risk_tier":"sensitive","rsid":"rs7895676","trait_name":"Cancer (standard GWA)","url":"https://www.mygenelog.com/variants/rs7895676"},{"risk_tier":"standard","rsid":"rs79184941","trait_name":"Acrocephalosyndactyly type I","url":"https://www.mygenelog.com/variants/rs79184941"},{"risk_tier":"sensitive","rsid":"rs879253719","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs879253719"},{"risk_tier":"sensitive","rsid":"rs879253721","trait_name":"Pfeiffer syndrome","url":"https://www.mygenelog.com/variants/rs879253721"}]}
