Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104886003
rs104886003
PIK3CA
A 0.700 CausalMutation CLINVAR

dbSNP: rs112445441
rs112445441
KRAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
PIK3CA
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
PIK3CA
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913286
rs121913286
PIK3CA
G 0.700 CausalMutation CLINVAR

dbSNP: rs28934874
rs28934874
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs28934874
rs28934874
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913500
rs121913500
IDH1
0.010 GeneticVariation BEFREE We describe the first reported case of an IDH1 p.R132L mutation in a patient with hormone receptor-positive (HR+) breast adenocarcinoma. 24760710

2014
dbSNP: rs121912664
rs121912664
TP53
0.010 GeneticVariation BEFREE Moreover, loss of heterozygocity with retention of the R337H allele was observed in a breast adenocarcinoma, supporting a role for this mutation in breast tumorigenesis. 16494995

2007