Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR Central European BRCA2 mutation carriers: birth cohort status correlates with onset of breast cancer. 24156927

2014
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Greece. 22085629

2011
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patients. 21120943

2011
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes. 21702907

2011
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristics. 20373018

2010
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 GeneticVariation CLINVAR Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. 11179017

2001
dbSNP: rs80359439
rs80359439
BRCA2
AT 0.700 CausalMutation CLINVAR