Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28897743
rs28897743
BRCA2
0.710 GeneticVariation BEFREE We have successfully identified a novel, germline heterozygous, missense mutation of the gene BRCA2: c.7007G>T, p.R2336L, which is likely to be pathogenic in the proband and her elder sister who both had breast cancer. 31782247

2020
dbSNP: rs28897743
rs28897743
BRCA2
C 0.710 CausalMutation CLINVAR

dbSNP: rs28897743
rs28897743
BRCA2
A 0.710 CausalMutation CLINVAR