rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
ACT |
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 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
ACT |
0.700 |
CausalMutation
|
CLINVAR |
Addressing health disparities in Hispanic breast cancer: accurate and inexpensive sequencing of BRCA1 and BRCA2.
|
26543556 |
2015 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Mutations of the BRCA1 gene in hereditary breast and ovarian cancer in the Czech Republic.
|
12566964 |
2003 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies.
|
15994883 |
2005 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Two distinct origins of a common BRCA1 mutation in breast-ovarian cancer families: a genetic study of 15 185delAG-mutation kindreds.
|
8651293 |
1996 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
ACT |
0.700 |
CausalMutation
|
CLINVAR |
Comprehensive Analysis of Germline Variants in Mexican Patients with Hereditary Breast and Ovarian Cancer Susceptibility.
|
30262796 |
2018 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.
|
9145676 |
1997 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Germline BRCA1 185delAG mutations in Jewish women with breast cancer.
|
8642955 |
1996 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Haplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations.
|
22763381 |
2013 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families.
|
7894492 |
1994 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women.
|
9042909 |
1997 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
High prevalence of BRCA1 and BRCA2 germline mutations with loss of heterozygosity in a series of resected pancreatic adenocarcinoma and other neoplastic lesions.
|
23658460 |
2013 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening.
|
7837387 |
1995 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.
|
8571953 |
1996 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish population.
|
20924075 |
2011 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriers.
|
22430266 |
2012 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Common BRCA1 and BRCA2 mutations in breast cancer families: a meta-analysis from systematic review.
|
21643751 |
2012 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Prevalence of the BRCA1 c.68_69delAG (BIC: 185delAG) mutation in women with breast cancer from north-central Poland and a review of the literature on other regions of the country.
|
23788959 |
2013 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
A high-throughput functional complementation assay for classification of BRCA1 missense variants.
|
23867111 |
2013 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
ACT |
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 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
BRCA1 and BRCA2 germline mutations are frequently demonstrated in both high-risk pancreatic cancer screening and pancreatic cancer cohorts.
|
24737347 |
2014 |
rs80357914
|
|
Hereditary Breast and Ovarian Cancer Syndrome
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Identification of the 185delAG BRCA1 mutation in a Spanish Gypsy population.
|
9921907 |
1998 |