Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79728106
rs79728106
T 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80358407
rs80358407
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80358407
rs80358407
A 0.700 CausalMutation CLINVAR Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR). 28726806

2018

dbSNP: rs80358547
rs80358547
G 0.700 CausalMutation CLINVAR Location of Mutation in BRCA2 Gene and Survival in Patients with Ovarian Cancer. 29084914

2018

dbSNP: rs80358593
rs80358593
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80358695
rs80358695
T 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80358809
rs80358809
A 0.700 CausalMutation CLINVAR Clinical genetic testing outcome with multi-gene panel in Asian patients with multiple primary cancers. 30093976

2018

dbSNP: rs80359013
rs80359013
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: rs80359014
rs80359014
T 0.700 GeneticVariation CLINVAR Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer. 29368341

2018

dbSNP: rs80359146
rs80359146
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80359159
rs80359159
T 0.700 CausalMutation CLINVAR The germline mutational landscape of BRCA1 and BRCA2 in Brazil. 29907814

2018

dbSNP: rs80359159
rs80359159
T 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: rs80359198
rs80359198
G 0.700 GeneticVariation CLINVAR Ipilimumab plus nivolumab and DNA-repair defects in AR-V7-expressing metastatic prostate cancer. 29983880

2018

dbSNP: rs80359198
rs80359198
G 0.700 GeneticVariation CLINVAR Germline DNA-repair Gene Mutations and Outcomes in Men with Metastatic Castration-resistant Prostate Cancer Receiving First-line Abiraterone and Enzalutamide. 29439820

2018

dbSNP: rs80359198
rs80359198
G 0.700 GeneticVariation CLINVAR Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer. 29368341

2018

dbSNP: rs80359198
rs80359198
G 0.700 GeneticVariation CLINVAR Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. 29394989

2018

dbSNP: rs80359211
rs80359211
A 0.700 CausalMutation CLINVAR Mutation analysis of BRCA1/2 mutations with special reference to polymorphic SNPs in Indian breast cancer patients. 29785135

2018

dbSNP: rs80359314
rs80359314
TAA 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80359334
rs80359334
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80359425
rs80359425
T 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: rs80359433
rs80359433
C 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80359444
rs80359444
A 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80359457
rs80359457
C 0.700 CausalMutation CLINVAR Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. 29446198

2018

dbSNP: rs80359459
rs80359459
C 0.700 CausalMutation CLINVAR Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer. 29368341

2018

dbSNP: rs80359503
rs80359503
A 0.700 CausalMutation CLINVAR BRCA germline mutations in an unselected nationwide cohort of Chinese patients with ovarian cancer and healthy controls. 30078507

2018