Gene: PALB2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555461176
rs1555461176
PALB2
AT 0.700 CausalMutation CLINVAR

dbSNP: rs587776416
rs587776416
PALB2
C 0.700 CausalMutation CLINVAR

dbSNP: rs879254154
rs879254154
PALB2
0.010 GeneticVariation BEFREE The proband carrier of c.3047T>C (p.F1016S) showed two breast cancer cases, two ovarian cancer cases and one pancreatic cancer in mother's family. c.3047T>C (p.F1016S) and c.*146A>G should be considered PALB2 UVs even though the genotype-phenotype correlation for these variants remains still unclear. 25666743

2015