Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886040914
rs886040914
G 0.700 GeneticVariation CLINVAR

dbSNP: rs886040913
rs886040913
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886040898
rs886040898
T 0.700 CausalMutation CLINVAR Molecular analysis of the BRCA1 and BRCA2 genes in 32 breast and/or ovarian cancer Spanish families. 10755399

2000

dbSNP: rs886040294
rs886040294
C 0.700 CausalMutation CLINVAR

dbSNP: rs886040282
rs886040282
T 0.700 CausalMutation CLINVAR

dbSNP: rs886040251
rs886040251
T 0.700 CausalMutation CLINVAR

dbSNP: rs886040241
rs886040241
A 0.700 CausalMutation CLINVAR

dbSNP: rs886040218
rs886040218
A 0.700 CausalMutation CLINVAR

dbSNP: rs886040205
rs886040205
GA 0.700 CausalMutation CLINVAR

dbSNP: rs886040185
rs886040185
A 0.700 CausalMutation CLINVAR

dbSNP: rs886040181
rs886040181
C 0.700 CausalMutation CLINVAR Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO). 22762150

2012

dbSNP: rs886040146
rs886040146
T 0.700 CausalMutation CLINVAR

dbSNP: rs886040129
rs886040129
G 0.700 CausalMutation CLINVAR

dbSNP: rs886040100
rs886040100
A 0.700 CausalMutation CLINVAR Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO). 22762150

2012

dbSNP: rs886040069
rs886040069
TG 0.700 CausalMutation CLINVAR

dbSNP: rs886040062
rs886040062
T 0.700 CausalMutation CLINVAR

dbSNP: rs886040027
rs886040027
TA 0.700 CausalMutation CLINVAR

dbSNP: rs886040009
rs886040009
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039987
rs886039987
T 0.700 CausalMutation CLINVAR Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO). 22762150

2012

dbSNP: rs886039987
rs886039987
T 0.700 CausalMutation CLINVAR Mutational analysis of BRCA1 and BRCA2 in hereditary breast and ovarian cancer families from Asturias (Northern Spain). 23683081

2013

dbSNP: rs886039982
rs886039982
T 0.700 CausalMutation CLINVAR

dbSNP: rs886039955
rs886039955
T 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: rs886039946
rs886039946
A 0.700 CausalMutation CLINVAR

dbSNP: rs886037998
rs886037998
C 0.700 CausalMutation CLINVAR

dbSNP: rs886037981
rs886037981
G 0.700 CausalMutation CLINVAR