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rs276174900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs276174900(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363204
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174900
ebirs276174900
HLIrs276174900
Exacrs276174900
Varsomers276174900
Maprs276174900
PheGenIrs276174900
hapmaprs276174900
1000 genomesrs276174900
hgdprs276174900
ensemblrs276174900
gopubmedrs276174900
geneviewrs276174900
scholarrs276174900
googlers276174900
pharmgkbrs276174900
gwascentralrs276174900
openSNPrs276174900
23andMers276174900
23andMe allrs276174900
SNP Nexus

SNPshotrs276174900
SNPdbers276174900
MSV3drs276174900
GWAS Ctlgrs276174900
Max Magnitude6
rs276174900, also known as A2668X, c.8002A>T and p.Arg2668Ter, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174900(G,T;G,T)
Alt rs276174900(G,T;G,T)
Reference rs276174900(A;A)
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.32937341A>T
CLNSRC ClinVar
CLNACC RCV000045382.2, RCV000113855.1,