rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
G
0.700
CausalMutation
CLINVAR
Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian study.
27062684
2016
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
G
0.700
CausalMutation
CLINVAR
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
25525159
2015
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
G
0.700
CausalMutation
CLINVAR
Comparative in vitro and in silico analyses of variants in splicing regions of BRCA1 and BRCA2 genes and characterization of novel pathogenic mutations.
23451180
2013
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
G
0.700
CausalMutation
CLINVAR
A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).
21990134
2012
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
G
0.700
CausalMutation
CLINVAR
Comprehensive prediction of mRNA splicing effects of BRCA1 and BRCA2 variants.
21523855
2011
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
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
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
G
0.700
CausalMutation
CLINVAR
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
17924331
2007
rs81002853
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
C
0.700
CausalMutation
CLINVAR