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rs276174910

From SNPedia

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


Make rs276174910(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376684
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174910
ebirs276174910
HLIrs276174910
Exacrs276174910
Varsomers276174910
Maprs276174910
PheGenIrs276174910
hapmaprs276174910
1000 genomesrs276174910
hgdprs276174910
ensemblrs276174910
gopubmedrs276174910
geneviewrs276174910
scholarrs276174910
googlers276174910
pharmgkbrs276174910
gwascentralrs276174910
openSNPrs276174910
23andMers276174910
23andMe allrs276174910
SNP Nexus

SNPshotrs276174910
SNPdbers276174910
MSV3drs276174910
GWAS Ctlgrs276174910
Max Magnitude6
rs276174910, also known as 8875delC, c.8647_8647delC and p.Pro2883Hisfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174910(;)
Alt rs276174910(;)
Reference rs276174910(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.32950821delC
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045591.2, RCV000113980.1,