Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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 Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. 28724667

2017
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas. 27767231

2017
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer. 28423363

2017
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Comparison of Targeted Next-Generation and Sanger Sequencing for the BRCA1 and BRCA2 Mutation Screening. 26709275

2016
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Identification of the prevalent BRCA1 and BRCA2 mutations in the female population of Puerto Rico. 22682623

2012
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Prevalence of BRCA1 and BRCA2 mutations in non-familial breast cancer patients with high risks in Korea: the Korean Hereditary Breast Cancer (KOHBRA) Study. 22382806

2012
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. 23199084

2010
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Germline mutations of BRCA1 and BRCA2 in Korean breast and/or ovarian cancer families. 12204006

2002
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations among Finnish ovarian carcinoma families. 11251181

2001
dbSNP: rs80358972
rs80358972
BRCA2
T 0.700 CausalMutation CLINVAR Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes. 9361038

1997