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rs276174864

From SNPedia

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


Make rs276174864(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340245
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174864
ebirs276174864
HLIrs276174864
Exacrs276174864
Varsomers276174864
Maprs276174864
PheGenIrs276174864
hapmaprs276174864
1000 genomesrs276174864
hgdprs276174864
ensemblrs276174864
gopubmedrs276174864
geneviewrs276174864
scholarrs276174864
googlers276174864
pharmgkbrs276174864
gwascentralrs276174864
openSNPrs276174864
23andMers276174864
23andMe allrs276174864
SNP Nexus

SNPshotrs276174864
SNPdbers276174864
MSV3drs276174864
GWAS Ctlgrs276174864
Max Magnitude6
rs276174864, also known as 6118delA, c.5890_5890delA and p.Lys1964Serfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174864(;)
Alt rs276174864(;)
Reference rs276174864(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.32914382delA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044785.2, RCV000113499.1,