Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Chromosome damage in G0 X-irradiated lymphocytes from patients with hereditary retinoblastoma. 6455195

1981
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR One Case of a BRCA1 Germ Line Mutation Ovarian Carcinoma Patient Based on Abnormal Immunohistochemistry Finding. 25366075

2014
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR [Simple and rapid technic of grouping of streptococci]. 824983

1976
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR AIDS legislation. 3175448

1988
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Purification and characterization of a new sodium-transport decarboxylase. Methylmalonyl-CoA decarboxylase from Veillonella alcalescens. 6852015

1983
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study. 25863477

2015
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR [The measuring for depth of papillary excavation by microcomputer (author's transl)]. 7257965

1980
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients. 15117986

2004
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer. 22798144

2012
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Diagnosis of vertebral fractures. 6848529

1983
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR BRCT repeats as phosphopeptide-binding modules involved in protein targeting. 14576432

2003
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Mutational analysis of a patient with mucopolysaccharidosis type VII, and identification of pseudogenes. 7680524

1993