rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Recurrent mutations of BRCA1, BRCA2 and PALB2 in the population of breast and ovarian cancer patients in Southern Poland.
|
26843898 |
2016 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing.
|
25366421 |
2015 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
|
24010542 |
2014 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive BRCA1 and BRCA2 mutational profile in Lithuania.
|
25066507 |
2014 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.
|
23479189 |
2013 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Common low-penetrance risk variants associated with breast cancer in Polish women.
|
24171766 |
2013 |
rs80357609
|
|
G |
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 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 regulates follistatin function in ovarian cancer and human ovarian surface epithelial cells.
|
22685544 |
2012 |
rs80357609
|
|
G |
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 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of the most frequent BRCA1 mutations in Polish population.
|
21503673 |
2011 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.
|
21702907 |
2011 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.
|
21324516 |
2011 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Non-founder BRCA1 mutations in Russian breast cancer patients.
|
20727672 |
2010 |
rs80357609
|
|
G |
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 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
[Prevalence of widespread BRCA1 gene mutations in patients with familial breast cancer from St. Petersburg].
|
15865297 |
2005 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.
|
16267036 |
2005 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic.
|
15024741 |
2004 |
rs80357609
|
|
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 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer.
|
10788334 |
2000 |
rs80357609
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutation analysis of the BRCA1 gene in ovarian cancers.
|
7606717 |
1995 |