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rs276174822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs276174822(-;-)
Make rs276174822(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position32336794
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174822
ebirs276174822
HLIrs276174822
Exacrs276174822
Varsomers276174822
Maprs276174822
PheGenIrs276174822
hapmaprs276174822
1000 genomesrs276174822
hgdprs276174822
ensemblrs276174822
gopubmedrs276174822
geneviewrs276174822
scholarrs276174822
googlers276174822
pharmgkbrs276174822
gwascentralrs276174822
openSNPrs276174822
23andMers276174822
23andMe allrs276174822
SNP Nexus

SNPshotrs276174822
SNPdbers276174822
MSV3drs276174822
GWAS Ctlgrs276174822
Max Magnitude6
rs276174822, also known as 2667insT, c.2439_2440insT and p.Ile813_Pro814?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174822(T;T)
Alt rs276174822(T;T)
Reference rs276174822(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910931dupT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000113043.1,