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rs276174826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CT) 6 BRCA2 variant considered pathogenic for breast cancer
(CT;CT) 0 common in clinvar


Make rs276174826(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336991
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174826
ebirs276174826
HLIrs276174826
Exacrs276174826
Varsomers276174826
Maprs276174826
PheGenIrs276174826
hapmaprs276174826
1000 genomesrs276174826
hgdprs276174826
ensemblrs276174826
gopubmedrs276174826
geneviewrs276174826
scholarrs276174826
googlers276174826
pharmgkbrs276174826
gwascentralrs276174826
openSNPrs276174826
23andMers276174826
23andMe allrs276174826
SNP Nexus

SNPshotrs276174826
SNPdbers276174826
MSV3drs276174826
GWAS Ctlgrs276174826
Max Magnitude6
rs276174826, also known as 2864delCT, c.2636_2637delCT and p.Ser879Terfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174826(;)
Alt rs276174826(;)
Reference rs276174826(CT;CT)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911128_32911129delCT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044029.2, RCV000113072.1,