Gene: BRCA1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR [Mutational analysis of BRCA1 and BRCA2 genes in early-onset breast cancer patients in Shanghai]. 16324400

2005
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR [Analysis of the mutations of BRCA1 in 9 familiar breast cancer patients]. 12947551

2003
dbSNP: rs786202791
rs786202791
BRCA1
T 0.700 CausalMutation CLINVAR [Analysis of mutations in genes BRCA1 and BRCA2 among patients with breast and ovarian cancer in northern Portugal and Galicia]. 12060539

2002
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR [5589del8: the recurrent mutation of BRCA1 gene in Chinese breast cancer patients]. 17680524

2007
dbSNP: rs397508939
rs397508939
BRCA1
T 0.700 CausalMutation CLINVAR Younger birth cohort correlates with higher breast and ovarian cancer risk in European BRCA1 mutation carriers. 16287141

2005
dbSNP: rs397509286
rs397509286
BRCA1
C 0.700 CausalMutation CLINVAR Younger birth cohort correlates with higher breast and ovarian cancer risk in European BRCA1 mutation carriers. 16287141

2005
dbSNP: rs80356888
rs80356888
BRCA1
T 0.700 CausalMutation CLINVAR Younger birth cohort correlates with higher breast and ovarian cancer risk in European BRCA1 mutation carriers. 16287141

2005
dbSNP: rs80357347
rs80357347
BRCA1
A 0.700 CausalMutation CLINVAR Younger birth cohort correlates with higher breast and ovarian cancer risk in European BRCA1 mutation carriers. 16287141

2005
dbSNP: rs80358018
rs80358018
BRCA1
T 0.700 CausalMutation CLINVAR Younger birth cohort correlates with higher breast and ovarian cancer risk in European BRCA1 mutation carriers. 16287141

2005
dbSNP: rs80357034
rs80357034
BRCA1
T 0.700 GeneticVariation CLINVAR Yeast cells reveal the misfolding and the cellular mislocalization of the human BRCA1 protein. 27802165

2016
dbSNP: rs80357971
rs80357971
BRCA1
G 0.700 CausalMutation CLINVAR When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans. 26884819

2016
dbSNP: rs397507215
rs397507215
BRCA1
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: rs730882165
rs730882165
BRCA1
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: rs80187739
rs80187739
BRCA1
G 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: rs80357318
rs80357318
BRCA1
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: rs80357389
rs80357389
BRCA1
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: rs80357433
rs80357433
BRCA1
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: rs80357461
rs80357461
BRCA1
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: rs80357575
rs80357575
BRCA1
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: rs80357902
rs80357902
BRCA1
AT 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: rs80357921
rs80357921
BRCA1
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: rs80359871
rs80359871
BRCA1 ; NBR2
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: rs863224510
rs863224510
BRCA1
TA 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
BRCA1
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: rs886040100
rs886040100
BRCA1
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