Gene: FGFR2 ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519854
rs1057519854
FGFR2
T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913475
rs121913475
FGFR2
C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913477
rs121913477
FGFR2
C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913478
rs121913478
FGFR2
C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs387906678
rs387906678
FGFR2
G 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs79184941
rs79184941
FGFR2
C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913477
rs121913477
FGFR2
C 0.700 GeneticVariation CLINVAR Targeting mutant fibroblast growth factor receptors in cancer. 21367659

2011
dbSNP: rs121913478
rs121913478
FGFR2
C 0.700 GeneticVariation CLINVAR Targeting mutant fibroblast growth factor receptors in cancer. 21367659

2011
dbSNP: rs79184941
rs79184941
FGFR2
C 0.700 GeneticVariation CLINVAR Targeting mutant fibroblast growth factor receptors in cancer. 21367659

2011
dbSNP: rs1057519901
rs1057519901
FGFR2
G 0.700 GeneticVariation CLINVAR Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. 17525745

2007
dbSNP: rs1057520027
rs1057520027
FGFR2
C 0.700 GeneticVariation CLINVAR Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. 17525745

2007
dbSNP: rs1057520028
rs1057520028
FGFR2
C 0.700 GeneticVariation CLINVAR Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. 17525745

2007
dbSNP: rs1057520029
rs1057520029
FGFR2
A 0.700 GeneticVariation CLINVAR Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. 17525745

2007