rs786203717
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer.
|
29368626 |
2018 |
rs876659533
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer.
|
29368626 |
2018 |
rs587780226
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Multigene panels in Ashkenazi Jewish patients yield high rates of actionable mutations in multiple non-BRCA cancer-associated genes.
|
28495237 |
2017 |
rs786203717
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
|
28423363 |
2017 |
rs1057519365
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.
|
27165003 |
2016 |
rs137852986
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
|
26921362 |
2016 |
rs587778134
|
|
CAA |
0.700 |
GeneticVariation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs587778134
|
|
CAA |
0.700 |
GeneticVariation |
CLINVAR |
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
|
26921362 |
2016 |
rs587778134
|
|
CAA |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587780224
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587780226
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs587780226
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587780226
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
|
26921362 |
2016 |
rs587780228
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inherited Mutations in Women With Ovarian Carcinoma.
|
26720728 |
2016 |
rs587780228
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587780236
|
|
TA |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs587781321
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
|
26786923 |
2016 |
rs587781321
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Inherited Mutations in Women With Ovarian Carcinoma.
|
26720728 |
2016 |
rs587781985
|
|
TC |
0.700 |
GeneticVariation |
CLINVAR |
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
|
27153395 |
2016 |
rs587782410
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
|
26921362 |
2016 |
rs730881649
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs730881649
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetic testing in a cohort of young patients with HER2-amplified breast cancer.
|
26681682 |
2016 |
rs730881649
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
|
26976419 |
2016 |
rs771028677
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
|
26921362 |
2016 |
rs779741278
|
|
CA |
0.700 |
GeneticVariation |
CLINVAR |
Monogenic and polygenic determinants of sarcoma risk: an international genetic study.
|
27498913 |
2016 |