BRCA1, BRCA1 DNA repair associated, 672

N. diseases: 747; N. variants: 2600
Disease: BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		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: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR Mutation screening of the BRCA1 gene in early onset and familial breast/ovarian cancer in Moroccan population. 23289006 2013
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR Hereditary breast cancer in Middle Eastern and North African (MENA) populations: identification of novel, recurrent and founder BRCA1 mutations in the Tunisian population. 21603858 2012
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations among ovarian cancer patients from Colombia. 22044689 2012
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516 2011
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study. 20104584 2010
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR BRCA1 mutations contribute to cell motility and invasion by affecting its main regulators. 19098453 2008
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR Frequency of germ-line BRCA1 mutations among Spanish families from a Mediterranean area. 10737987 2000
dbSNP: rs80357701
rs80357701
Entrez Id: 672
Gene Symbol: BRCA1
BRCA1
CUI: C2676676
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 		T 0.700 CausalMutation CLINVAR Mutation analysis of the BRCA1 gene in 23 families with cases of cancer of the breast, ovary, and multiple other sites. 8933332 1996