Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR High prevalence of BRCA1 founder mutations in Greek breast/ovarian families. 24010542

2014
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity. 22752604

2012
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR BRCA1 And BRCA2 analysis of Argentinean breastovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin. 23961350

2012
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311

2011
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects. 10227398

1999
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. 9150154

1997