rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
[Prevalence of widespread BRCA1 gene mutations in patients with familial breast cancer from St. Petersburg].
|
15865297 |
2005 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clustering of variations and haplotype analysis in the highly variable region of exon 11 of BRCA1 in Chinese women with sporadic breast cancer.
|
12402341 |
2002 |
rs62625308
|
|
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 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.
|
21324516 |
2011 |
rs62625308
|
|
A |
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 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of BRCA1 founder mutations in Greek breast/ovarian families.
|
24010542 |
2014 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients.
|
12655560 |
2003 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity.
|
22752604 |
2012 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
|
22006311 |
2011 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
|
25525159 |
2015 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Greek BRCA1 and BRCA2 mutation spectrum: two BRCA1 mutations account for half the carriers found among high-risk breast/ovarian cancer patients.
|
17453335 |
2008 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.
|
25452441 |
2015 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of BRCA1 mutations in familial and sporadic greek ovarian cancer cases.
|
23536787 |
2013 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations.
|
26028024 |
2016 |
rs62625308
|
|
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 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families.
|
7894493 |
1994 |
rs62625308
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
|
25637381 |
2015 |
rs62625308
|
|
A |
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 |