Gene: BRCA2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507422
rs397507422
BRCA2
C 0.700 CausalMutation CLINVAR Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population. 30630528

2019
dbSNP: rs397507884
rs397507884
BRCA2
G 0.700 CausalMutation CLINVAR Mis-splicing in breast cancer: identification of pathogenic BRCA2 variants by systematic minigene assays. 30883759

2019
dbSNP: rs80358843
rs80358843
BRCA2
G 0.700 CausalMutation CLINVAR BRCA Reversion Mutations in Circulating Tumor DNA Predict Primary and Acquired Resistance to the PARP Inhibitor Rucaparib in High-Grade Ovarian Carcinoma. 30425037

2019
dbSNP: rs80359013
rs80359013
BRCA2
C 0.700 CausalMutation CLINVAR The functional impact of variants of uncertain significance in BRCA2. 29988080

2019
dbSNP: rs80359519
rs80359519
BRCA2
C 0.700 CausalMutation CLINVAR Population and breast cancer patients' analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population. 30630528

2019
dbSNP: rs81002796
rs81002796
BRCA2
T 0.700 CausalMutation CLINVAR Mis-splicing in breast cancer: identification of pathogenic BRCA2 variants by systematic minigene assays. 30883759

2019
dbSNP: rs1466688245
rs1466688245
BRCA2
G 0.700 CausalMutation CLINVAR Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan. 29176636

2018
dbSNP: rs1566249353
rs1566249353
BRCA2
GA 0.700 CausalMutation CLINVAR Genetic and clinical characteristics in Japanese hereditary breast and ovarian cancer: first report after establishment of HBOC registration system in Japan. 29176636

2018
dbSNP: rs276174843
rs276174843
BRCA2
A 0.700 CausalMutation CLINVAR Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer. 29368341

2018
dbSNP: rs397507410
rs397507410
BRCA2
G 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs397507634
rs397507634
BRCA2
A 0.700 CausalMutation CLINVAR Location of Mutation in BRCA2 Gene and Survival in Patients with Ovarian Cancer. 29084914

2018
dbSNP: rs397507634
rs397507634
BRCA2
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs397507634
rs397507634
BRCA2
A 0.700 CausalMutation CLINVAR Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia. 28993434

2018
dbSNP: rs397507683
rs397507683
BRCA2
GA 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway. 29339979

2018
dbSNP: rs397507788
rs397507788
BRCA2
T 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs397507865
rs397507865
BRCA2
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs397507868
rs397507868
BRCA2
T 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs397507884
rs397507884
BRCA2
G 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs55996097
rs55996097
BRCA2
T 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs587782011
rs587782011
BRCA2
G 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018
dbSNP: rs587782854
rs587782854
BRCA2
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway. 29339979

2018
dbSNP: rs750385844
rs750385844
BRCA2
T 0.700 CausalMutation CLINVAR Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations. 29470806

2018
dbSNP: rs758732038
rs758732038
BRCA2
C 0.700 GeneticVariation CLINVAR Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia. 28993434

2018
dbSNP: rs786201180
rs786201180
BRCA2
T 0.700 CausalMutation CLINVAR Characterization of spliceogenic variants located in regions linked to high levels of alternative splicing: BRCA2 c.7976+5G > T as a case study. 29969168

2018
dbSNP: rs79728106
rs79728106
BRCA2
T 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018