Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853079
rs137853079
A 0.700 CausalMutation CLINVAR

dbSNP: rs397518442
rs397518442
T 0.700 CausalMutation CLINVAR

dbSNP: rs397518443
rs397518443
G 0.700 CausalMutation CLINVAR

dbSNP: rs730881976
rs730881976
G 0.700 GeneticVariation CLINVAR

dbSNP: rs375328708
rs375328708
0.010 GeneticVariation BEFREE One silent change, C1257T, was found in a pancreatic carcinoma sample. 10079245

1999