Gene: BRCA2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359066
rs80359066
BRCA2
C 0.700 GeneticVariation CLINVAR Genomic Heterogeneity Within Individual Prostate Cancer Foci Impacts Predictive Biomarkers of Targeted Therapy. 29398457

2019
dbSNP: rs80359527
rs80359527
BRCA2
TA 0.700 CausalMutation CLINVAR Synchronous Onset of Breast and Pancreatic Cancers: Results of Germline and Somatic Genetic Analysis. 27721756

2019
dbSNP: rs28897743
rs28897743
BRCA2
A 0.700 CausalMutation CLINVAR High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients. 29297111

2018
dbSNP: rs28897743
rs28897743
BRCA2
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs28897746
rs28897746
BRCA2
C 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs397507375
rs397507375
BRCA2
C 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs41293511
rs41293511
BRCA2
C 0.700 CausalMutation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs41293513
rs41293513
BRCA2
T 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs41293513
rs41293513
BRCA2
G 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia. 29335924

2018
dbSNP: rs80358721
rs80358721
BRCA2
G 0.700 CausalMutation CLINVAR Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds. 29371908

2018
dbSNP: rs80358972
rs80358972
BRCA2
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
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Detection of Germline Mutations in Patients with Epithelial Ovarian Cancer Using Multi-gene Panels: Beyond BRCA1/2. 29020732

2018
dbSNP: rs80358979
rs80358979
BRCA2
C 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359009
rs80359009
BRCA2
T 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359012
rs80359012
BRCA2
G 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359013
rs80359013
BRCA2
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
dbSNP: rs80359013
rs80359013
BRCA2
C 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359014
rs80359014
BRCA2
T 0.700 GeneticVariation CLINVAR BRCA1 and BRCA2 germline variants in breast cancer patients from the Republic of Macedonia. 29335924

2018
dbSNP: rs80359024
rs80359024
BRCA2
G 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359035
rs80359035
BRCA2
T 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359064
rs80359064
BRCA2
G 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359075
rs80359075
BRCA2
T 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359082
rs80359082
BRCA2
A 0.700 CausalMutation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359083
rs80359083
BRCA2
A 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018
dbSNP: rs80359152
rs80359152
BRCA2
A 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018