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rs276174833

From SNPedia

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


Make rs276174833(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337632
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174833
ebirs276174833
HLIrs276174833
Exacrs276174833
Varsomers276174833
Maprs276174833
PheGenIrs276174833
hapmaprs276174833
1000 genomesrs276174833
hgdprs276174833
ensemblrs276174833
gopubmedrs276174833
geneviewrs276174833
scholarrs276174833
googlers276174833
pharmgkbrs276174833
gwascentralrs276174833
openSNPrs276174833
23andMers276174833
23andMe allrs276174833
SNP Nexus

SNPshotrs276174833
SNPdbers276174833
MSV3drs276174833
GWAS Ctlgrs276174833
Max Magnitude6
rs276174833, also known as 3505delT, c.3277_3277delT and p.Ser1093Profs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174833(;)
Alt rs276174833(;)
Reference rs276174833(T;T)
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.32911769delT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044169.2, RCV000113158.1,