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rs276174890

From SNPedia

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


Make rs276174890(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355004
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174890
ebirs276174890
HLIrs276174890
Exacrs276174890
Varsomers276174890
Maprs276174890
PheGenIrs276174890
hapmaprs276174890
1000 genomesrs276174890
hgdprs276174890
ensemblrs276174890
gopubmedrs276174890
geneviewrs276174890
scholarrs276174890
googlers276174890
pharmgkbrs276174890
gwascentralrs276174890
openSNPrs276174890
23andMers276174890
23andMe allrs276174890
SNP Nexus

SNPshotrs276174890
SNPdbers276174890
MSV3drs276174890
GWAS Ctlgrs276174890
Max Magnitude6
rs276174890, also known as 7379delAA, c.7151_7152delAA and p.Gln2384Argfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174890(;)
Alt rs276174890(;)
Reference rs276174890(AA;AA)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32929141_32929142delAA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045150.2, RCV000113713.1, RCV000162935.1,