Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359406
rs80359406
BRCA2
G 0.700 GeneticVariation CLINVAR RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins. 26635394

2016
dbSNP: rs80359406
rs80359406
BRCA2
G 0.700 CausalMutation CLINVAR Central European BRCA2 mutation carriers: birth cohort status correlates with onset of breast cancer. 24156927

2014
dbSNP: rs80359406
rs80359406
BRCA2
GA 0.700 CausalMutation CLINVAR A BRCA2 mutation, 4088insA, in a Finnish breast and ovarian cancer family associated with favourable clinical course. 18214034

2008
dbSNP: rs80359406
rs80359406
BRCA2
GA 0.700 CausalMutation CLINVAR Histopathological features of breast tumours in BRCA1, BRCA2 and mutation-negative breast cancer families. 15642173

2005
dbSNP: rs80359406
rs80359406
BRCA2
G 0.700 CausalMutation CLINVAR Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects. 12955716

2003
dbSNP: rs80359406
rs80359406
BRCA2
G 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland. 12673801

2003