rs80359066
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Genomic Heterogeneity Within Individual Prostate Cancer Foci Impacts Predictive Biomarkers of Targeted Therapy.
|
29398457 |
2019 |
rs80359527
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Synchronous Onset of Breast and Pancreatic Cancers: Results of Germline and Somatic Genetic Analysis.
|
27721756 |
2019 |
rs28897743
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs28897743
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients.
|
29297111 |
2018 |
rs28897746
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs397507375
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
|
29446198 |
2018 |
rs41293511
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs41293513
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs41293513
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.
|
29335924 |
2018 |
rs80358721
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
|
29371908 |
2018 |
rs80358972
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Detection of Germline Mutations in Patients with Epithelial Ovarian Cancer Using Multi-gene Panels: Beyond BRCA1/2.
|
29020732 |
2018 |
rs80358972
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline BRCA mutations in Asian patients with pancreatic adenocarcinoma: a prospective study evaluating risk category for genetic testing.
|
28782087 |
2018 |
rs80358979
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359009
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359012
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359013
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway.
|
29339979 |
2018 |
rs80359013
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359014
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia.
|
29335924 |
2018 |
rs80359024
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359035
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359064
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359075
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359082
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359083
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |
rs80359152
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches.
|
29394989 |
2018 |