rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer.
|
22798144 |
2012 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families.
|
22160602 |
2012 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy.
|
21989927 |
2012 |
rs80357580
|
|
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
|
ATTAG |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 genetic testing in 106 breast and ovarian cancer families from Southern Italy (Sicily): a mutation analyses.
|
17221156 |
2007 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer.
|
22798144 |
2012 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer.
|
22277901 |
2012 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
ATTAG |
0.700 |
CausalMutation
|
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy.
|
21989927 |
2012 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
A high proportion of founder BRCA1 mutations in Polish breast cancer families.
|
15146557 |
2004 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families.
|
22160602 |
2012 |
rs80357580
|
|
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
|
A |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.
|
9150149 |
1997 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.
|
9150149 |
1997 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.
|
9150149 |
1997 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
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 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients.
|
27553291 |
2016 |
rs80357580
|
|
Mammary Neoplasms
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients.
|
27257965 |
2016 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients.
|
26183948 |
2015 |
rs80357580
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases.
|
22144684 |
2012 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study.
|
25863477 |
2015 |
rs80357580
|
|
Neoplastic Syndromes, Hereditary
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases.
|
22144684 |
2012 |