Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567204928
rs1567204928
PALB2
CAA 0.700 CausalMutation CLINVAR Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapy. 26296701

2015
dbSNP: rs1567204928
rs1567204928
PALB2
CAA 0.700 CausalMutation CLINVAR Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. 26315354

2015
dbSNP: rs1567204928
rs1567204928
PALB2
CAA 0.700 CausalMutation CLINVAR PALB2 mutations in familial breast and pancreatic cancer. 21365267

2011
dbSNP: rs1567204928
rs1567204928
PALB2
CAA 0.700 CausalMutation CLINVAR Structural basis for recruitment of BRCA2 by PALB2. 19609323

2009
dbSNP: rs1567204928
rs1567204928
PALB2
CAA 0.700 CausalMutation CLINVAR Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. 17200671

2007