Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359773
rs80359773
BRCA2
TA 0.700 CausalMutation CLINVAR Biallelic FANCD1/BRCA2 mutations predisposing to glioblastoma multiforme with multiple oncogenic amplifications. 26740091

2016
dbSNP: rs80359773
rs80359773
BRCA2
TA 0.700 CausalMutation CLINVAR Central European BRCA2 mutation carriers: birth cohort status correlates with onset of breast cancer. 24156927

2014
dbSNP: rs80359773
rs80359773
BRCA2
TA 0.700 CausalMutation CLINVAR Support of the 'fallopian tube hypothesis' in a prospective series of risk-reducing salpingo-oophorectomy specimens. 22921157

2013
dbSNP: rs80359773
rs80359773
BRCA2
TA 0.700 CausalMutation CLINVAR Rad52 inactivation is synthetically lethal with BRCA2 deficiency. 21148102

2011
dbSNP: rs80359773
rs80359773
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: rs80359773
rs80359773
BRCA2
TA 0.700 CausalMutation CLINVAR Biallelic inactivation of BRCA2 in Fanconi anemia. 12065746

2002
dbSNP: rs80359773
rs80359773
BRCA2
TA 0.700 CausalMutation CLINVAR Cancer risks in BRCA2 mutation carriers. 10433620

1999