Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Genetic testing for BRCA1 and BRCA2 in the Province of Ontario. 26219728

2016

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer. 27067391

2016

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Absence of BRCA/FMR1 correlations in women with ovarian cancers. 25036526

2014

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes. 21702907

2011

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. 23199084

2010

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR BRCA1 5083del19 mutant allele selectively up-regulates periostin expression in vitro and in vivo. 18980973

2008

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups. 18159056

2007

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR BRCA1 genetic testing in 106 breast and ovarian cancer families from Southern Italy (Sicily): a mutation analyses. 17221156

2007

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Novel BRCA1 and BRCA2 germline mutations and assessment of mutation spectrum and prevalence in Italian breast and/or ovarian cancer families. 16847550

2006

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR BRCA mutations in Italian breast/ovarian cancer families. 11938448

2002

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR Evidence of a founder mutation of BRCA1 in a highly homogeneous population from southern Italy with breast/ovarian cancer. 11462242

2001

dbSNP: rs80359876
rs80359876
T 0.700 CausalMutation CLINVAR BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. 9145677

1997