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rs276174868

From SNPedia

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


Make rs276174868(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340622
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174868
ClinGenrs276174868
ebirs276174868
HLIrs276174868
Exacrs276174868
Varsomers276174868
Maprs276174868
PheGenIrs276174868
hapmaprs276174868
1000 genomesrs276174868
hgdprs276174868
ensemblrs276174868
gopubmedrs276174868
geneviewrs276174868
scholarrs276174868
googlers276174868
pharmgkbrs276174868
gwascentralrs276174868
openSNPrs276174868
23andMers276174868
23andMe allrs276174868
SNP Nexus

SNPshotrs276174868
SNPdbers276174868
MSV3drs276174868
GWAS Ctlgrs276174868
Max Magnitude6
rs276174868, also known as 6495delGCAinsC, c.6267_6269delGCAinsC and p.Glu2089_His2090AspTerfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174868(C;C)
Alt rs276174868(C;C)
Reference Rs276174868(GCA;GCA)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32914759_32914761delGCAinsC
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031610.7, RCV000044881.3, RCV000129598.3, RCV000254646.1,