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rs276174902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs276174902(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332287
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174902
ebirs276174902
HLIrs276174902
Exacrs276174902
Varsomers276174902
Maprs276174902
PheGenIrs276174902
hapmaprs276174902
1000 genomesrs276174902
hgdprs276174902
ensemblrs276174902
gopubmedrs276174902
geneviewrs276174902
scholarrs276174902
googlers276174902
pharmgkbrs276174902
gwascentralrs276174902
openSNPrs276174902
23andMers276174902
23andMe allrs276174902
SNP Nexus

SNPshotrs276174902
SNPdbers276174902
MSV3drs276174902
GWAS Ctlgrs276174902
Max Magnitude6
rs276174902, also known as S270X, c.809C>G and p.Ser270Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174902(G;G)
Alt rs276174902(G;G)
Reference rs276174902(C;C)
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.32906424C>G
CLNSRC ClinVar
CLNACC RCV000045422.2, RCV000112846.1,