Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1021662947
rs1021662947
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499812
rs1060499812
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499819
rs1060499819
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499824
rs1060499824
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499828
rs1060499828
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499829
rs1060499829
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499830
rs1060499830
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499831
rs1060499831
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502800
rs1060502800
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502804
rs1060502804
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1064795824
rs1064795824
A 0.700 CausalMutation CLINVAR

dbSNP: rs118203999
rs118203999
A 0.700 CausalMutation CLINVAR Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer. 21618343

2011

dbSNP: rs118203999
rs118203999
A 0.700 CausalMutation CLINVAR Exploring the roles of PALB2 at the crossroads of DNA repair and cancer. 24870022

2014

dbSNP: rs118203999
rs118203999
A 0.700 CausalMutation CLINVAR PALB2 mutations in familial breast and pancreatic cancer. 21365267

2011

dbSNP: rs118203999
rs118203999
A 0.700 CausalMutation CLINVAR Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. 17200671

2007

dbSNP: rs1219715328
rs1219715328
A 0.700 CausalMutation CLINVAR

dbSNP: rs1248579792
rs1248579792
A 0.700 CausalMutation CLINVAR

dbSNP: rs1327399690
rs1327399690
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555459386
rs1555459386
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555459999
rs1555459999
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555460323
rs1555460323
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555460431
rs1555460431
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555460445
rs1555460445
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555460445
rs1555460445
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555460526
rs1555460526
A 0.700 CausalMutation CLINVAR