Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79184941
rs79184941
C 0.710 CausalMutation CLINVAR

dbSNP: rs79184941
rs79184941
0.710 GeneticVariation BEFREE FGFR2 exons 7 and 12 unlabeled DNA probes allow for easy screening of endometrial carcinoma for the 2 most common FGFR2 mutations (S252W and N550K). 21285871

2011