Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs180177132
rs180177132
T 0.730 CausalMutation CLINVAR About 1.5% (95% CI 0.6to 2.4) of Australasian multiple-case breast cancer families attending clinics are segregating protein-truncating mutations in PALB2, most being PALB2 c.3113G>A, p.Trp1038*. 23448497

2013

dbSNP: rs180177132
rs180177132
T 0.730 CausalMutation CLINVAR Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. 21285249

2011

dbSNP: rs180177132
rs180177132
T 0.730 CausalMutation CLINVAR Further screening for PALB2 c.3113G > A (W1038X) was conducted for 779 families with multiple cases of breast cancer ascertained through family cancer clinics in Australia and New Zealand and 764 population-based controls. 21182766

2010

dbSNP: rs515726123
rs515726123
A 0.710 CausalMutation CLINVAR Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. 21285249

2011

dbSNP: rs515726123
rs515726123
A 0.710 CausalMutation CLINVAR PALB2 mutations in European familial pancreatic cancer families. 20412113

2010

dbSNP: rs515726123
rs515726123
A 0.710 CausalMutation CLINVAR A novel germline PALB2 deletion in Polish breast and ovarian cancer patients. 20122277

2010

dbSNP: rs180177133
rs180177133
A 0.700 CausalMutation CLINVAR

dbSNP: rs769240800
rs769240800
C 0.700 CausalMutation CLINVAR