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rs276174875

From SNPedia

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


Make rs276174875(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341028
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174875
ebirs276174875
HLIrs276174875
Exacrs276174875
Varsomers276174875
Maprs276174875
PheGenIrs276174875
hapmaprs276174875
1000 genomesrs276174875
hgdprs276174875
ensemblrs276174875
gopubmedrs276174875
geneviewrs276174875
scholarrs276174875
googlers276174875
pharmgkbrs276174875
gwascentralrs276174875
openSNPrs276174875
23andMers276174875
23andMe allrs276174875
SNP Nexus

SNPshotrs276174875
SNPdbers276174875
MSV3drs276174875
GWAS Ctlgrs276174875
Max Magnitude6
rs276174875, also known as 6901delA, c.6673_6673delA and p.Thr2225Glnfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174875(;)
Alt rs276174875(;)
Reference rs276174875(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.32915165delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045013.2, RCV000113625.1,