Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359527
rs80359527
BRCA2
TA 0.700 CausalMutation CLINVAR BRCA1 And BRCA2 analysis of Argentinean breastovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin. 23961350

2012
dbSNP: rs80359527
rs80359527
BRCA2
TA 0.700 CausalMutation CLINVAR The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: two recurrent mutations were identified. 17851763

2008
dbSNP: rs80359527
rs80359527
BRCA2
TA 0.700 CausalMutation CLINVAR Breast cancer risk among male BRCA1 and BRCA2 mutation carriers. 18042939

2007
dbSNP: rs80359527
rs80359527
BRCA2
TA 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: rs80359527
rs80359527
BRCA2
TA 0.700 CausalMutation CLINVAR Contribution of BRCA2 germline mutations to hereditary breast/ovarian cancer in Germany. 11897832

2002
dbSNP: rs80359527
rs80359527
BRCA2
TA 0.700 CausalMutation CLINVAR An improved high throughput heteroduplex mutation detection system for screening BRCA2 mutations-fluorescent mutation detection (F-MD). 11241844

2001