Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity. 22752604

2012
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR Identification of BRCA1/2 founder mutations in Southern Chinese breast cancer patients using gene sequencing and high resolution DNA melting analysis. 22970155

2012
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR A BRCA2 founder mutation and seven novel deleterious BRCA mutations in southern Chinese women with breast and ovarian cancer. 19353265

2009
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR BRCA1 and BRCA2 germline mutation analysis among Indian women from south India: identification of four novel mutations and high-frequency occurrence of 185delAG mutation. 19805903

2009
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy. 18821011

2009
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR Cancer variation associated with the position of the mutation in the BRCA2 gene. 15131399

2004
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 GeneticVariation CLINVAR Characterization of ten novel and 13 recurring BRCA1 and BRCA2 germline mutations in Italian breast and/or ovarian carcinoma patients. Mutations in brief no. 178. Online. 10660329

1998
dbSNP: rs80359543
rs80359543
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80359543
rs80359543
BRCA2
TGTTA 0.700 CausalMutation CLINVAR