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rs276174860

From SNPedia

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


Make rs276174860(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339996
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174860
ebirs276174860
HLIrs276174860
Exacrs276174860
Varsomers276174860
Maprs276174860
PheGenIrs276174860
hapmaprs276174860
1000 genomesrs276174860
hgdprs276174860
ensemblrs276174860
gopubmedrs276174860
geneviewrs276174860
scholarrs276174860
googlers276174860
pharmgkbrs276174860
gwascentralrs276174860
openSNPrs276174860
23andMers276174860
23andMe allrs276174860
SNP Nexus

SNPshotrs276174860
SNPdbers276174860
MSV3drs276174860
GWAS Ctlgrs276174860
Max Magnitude6
rs276174860, also known as 5869delAAAT, c.5641_5644delAAAT and p.Lys1881_Ser1882?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174860(;)
Alt rs276174860(;)
Reference rs276174860(AATA;AATA)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32914133_32914136delAAAT
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000074542.5, RCV000113451.3, RCV000235141.1,