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rs81002868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002868(A;C)
Make rs81002868(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32396896
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002868
ebirs81002868
HLIrs81002868
Exacrs81002868
Varsomers81002868
Maprs81002868
PheGenIrs81002868
hapmaprs81002868
1000 genomesrs81002868
hgdprs81002868
ensemblrs81002868
gopubmedrs81002868
geneviewrs81002868
scholarrs81002868
googlers81002868
pharmgkbrs81002868
gwascentralrs81002868
openSNPrs81002868
23andMers81002868
23andMe allrs81002868
SNP Nexus

SNPshotrs81002868
SNPdbers81002868
MSV3drs81002868
GWAS Ctlgrs81002868
Max Magnitude0
ClinVar
Risk rs81002868(C;C)
Alt rs81002868(C;C)
Reference rs81002868(A;A)
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.32971033A>C
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045844.2, RCV000114124.1, RCV000131049.2,