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rs276174901

From SNPedia

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


Make rs276174901(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363244
GeneBRCA2
is asnp
is mentioned by
dbSNPrs276174901
ebirs276174901
HLIrs276174901
Exacrs276174901
Varsomers276174901
Maprs276174901
PheGenIrs276174901
hapmaprs276174901
1000 genomesrs276174901
hgdprs276174901
ensemblrs276174901
gopubmedrs276174901
geneviewrs276174901
scholarrs276174901
googlers276174901
pharmgkbrs276174901
gwascentralrs276174901
openSNPrs276174901
23andMers276174901
23andMe allrs276174901
SNP Nexus

SNPshotrs276174901
SNPdbers276174901
MSV3drs276174901
GWAS Ctlgrs276174901
Max Magnitude6
rs276174901, also known as 8270delCA, c.8042_8043delCA and p.Thr2681Serfs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.
ClinVar
Risk rs276174901(;)
Alt rs276174901(;)
Reference rs276174901(AC;AC)
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.32937381_32937382delCA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045399.2, RCV000077425.3,