Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28934874
rs28934874
A 0.700 CausalMutation CLINVAR

dbSNP: rs28934874
rs28934874
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912664
rs121912664
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