Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80358815
rs80358815
A 0.700 CausalMutation CLINVAR Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients. 26483394

2016

dbSNP: rs80358815
rs80358815
A 0.700 CausalMutation CLINVAR Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. 24504028

2014

dbSNP: rs80358815
rs80358815
A 0.700 CausalMutation CLINVAR "Methylation not a frequent ""second hit"" in tumors with germline BRCA mutations." 19340607

2009

dbSNP: rs80358815
rs80358815
A 0.700 GeneticVariation CLINVAR "Methylation not a frequent ""second hit"" in tumors with germline BRCA mutations." 19340607

2009

dbSNP: rs80358815
rs80358815
A 0.700 CausalMutation CLINVAR A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting. 16683254

2006

dbSNP: rs80358815
rs80358815
A 0.700 GeneticVariation CLINVAR Cancer variation associated with the position of the mutation in the BRCA2 gene. 15131399

2004

dbSNP: rs80358815
rs80358815
A 0.700 CausalMutation CLINVAR Cancer variation associated with the position of the mutation in the BRCA2 gene. 15131399

2004

dbSNP: rs80358815
rs80358815
A 0.700 CausalMutation CLINVAR Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population. 11802209

2002

dbSNP: rs80358815
rs80358815
A 0.700 GeneticVariation CLINVAR Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population. 11802209

2002

dbSNP: rs80358815
rs80358815
G 0.700 CausalMutation CLINVAR