|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Overall survival and clinical characteristics of pancreatic cancer in BRCA mutation carriers.
|
25072261 |
2014 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Mutational analysis of BRCA1 and BRCA2 in hereditary breast and ovarian cancer families from Asturias (Northern Spain).
|
23683081 |
2013 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management.
|
22535016 |
2012 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
A 24-color metaphase-based radiation assay discriminates heterozygous BRCA2 mutation carriers from controls by chromosomal radiosensitivity.
|
22729890 |
2012 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
G |
0.700 |
CausalMutation
|
CLINVAR |
High grade prostatic intraepithelial neoplasia does not display loss of heterozygosity at the mutation locus in BRCA2 mutation carriers with aggressive prostate cancer.
|
23035815 |
2012 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population.
|
21232165 |
2011 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients.
|
21952622 |
2011 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.
|
21324516 |
2011 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
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 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.
|
23199084 |
2010 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer.
|
18489799 |
2008 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Cross-sectional analysis of germline BRCA1 and BRCA2 mutations in Japanese patients suspected to have hereditary breast/ovarian cancer.
|
19016756 |
2008 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Breast cancer risk among male BRCA1 and BRCA2 mutation carriers.
|
18042939 |
2007 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour.
|
15689453 |
2005 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia.
|
15070707 |
2004 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic.
|
15024741 |
2004 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Analysis of breast cancer susceptibility genes BRCA1 and BRCA2 in Thai familial and isolated early-onset breast and ovarian cancer.
|
12203997 |
2002 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population.
|
11802209 |
2002 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
G |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.
|
11389159 |
2001 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Detection of BRCA1 and BRCA2 mutations in breast cancer families by a comprehensive two-stage screening procedure.
|
10699917 |
2000 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.
|
9667259 |
1998 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.
|
9585613 |
1998 |
|
rs80359306
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
GA |
0.700 |
CausalMutation
|
CLINVAR |
BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.
|
9150150 |
1997 |