Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR A high frequency of PALB2 mutations in Jamaican patients with breast cancer. 28194609

2017
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls. 26283626

2015
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754

2015
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Inherited predisposition to breast cancer among African American women. 25428789

2015
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Low prevalence of germline PALB2 mutations in Australian triple-negative breast cancer. 23824750

2014
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. 24763289

2014
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Novel germline PALB2 truncating mutations in African American breast cancer patients. 21932393

2012
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 CausalMutation CLINVAR Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer. 23110154

2012
dbSNP: rs515726126
rs515726126
PALB2
TA 0.700 GeneticVariation CLINVAR