rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
|
27836010 |
2016 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status.
|
24504028 |
2014 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2.
|
26360800 |
2016 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Survival in hereditary breast cancer associated with germline mutations of BRCA2.
|
10550133 |
1999 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Detection of BRCA1 and BRCA2 mutations in breast cancer families by a comprehensive two-stage screening procedure.
|
10699917 |
2000 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.
|
21324516 |
2011 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Variation in cancer risks, by mutation position, in BRCA2 mutation carriers.
|
11170890 |
2001 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population.
|
21232165 |
2011 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
|
16683254 |
2006 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.
|
23569316 |
2013 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.
|
9585613 |
1998 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene.
|
8988179 |
1997 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
|
22006311 |
2011 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer.
|
22798144 |
2012 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Nonequivalent gene expression and copy number alterations in high-grade serous ovarian cancers with BRCA1 and BRCA2 mutations.
|
23633455 |
2013 |
rs80359507
|
|
CA |
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 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.
|
23199084 |
2010 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
|
22006311 |
2011 |
rs80359507
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada.
|
17148771 |
2006 |
rs80359507
|
|
C |
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 |
rs80359507
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families.
|
10638982 |
2000 |