Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359343
rs80359343
BRCA2
G 0.700 CausalMutation CLINVAR Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles. 23028338

2012
dbSNP: rs80359343
rs80359343
BRCA2
G 0.700 CausalMutation CLINVAR BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study Group. 22711857

2012
dbSNP: rs80359343
rs80359343
BRCA2
G 0.700 CausalMutation CLINVAR BRCA1/2 mutation analysis in male breast cancer families from North West England. 17636422

2008
dbSNP: rs80359343
rs80359343
BRCA2
G 0.700 CausalMutation CLINVAR Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. 8988179

1997
dbSNP: rs80359343
rs80359343
BRCA2
G 0.700 CausalMutation CLINVAR The cultural reasons underlying this meeting. 3413277

1988
dbSNP: rs80359343
rs80359343
BRCA2
G 0.700 CausalMutation CLINVAR Room air ventilation for total intravenous general anaesthesia. 3146935

1988