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rs81002849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs81002849(A;A)
Make rs81002849(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326498
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002849
ebirs81002849
HLIrs81002849
Exacrs81002849
Varsomers81002849
Maprs81002849
PheGenIrs81002849
hapmaprs81002849
1000 genomesrs81002849
hgdprs81002849
ensemblrs81002849
gopubmedrs81002849
geneviewrs81002849
scholarrs81002849
googlers81002849
pharmgkbrs81002849
gwascentralrs81002849
openSNPrs81002849
23andMers81002849
23andMe allrs81002849
SNP Nexus

SNPshotrs81002849
SNPdbers81002849
MSV3drs81002849
GWAS Ctlgrs81002849
Max Magnitude0
ClinVar
Risk rs81002849(A;A)
Alt rs81002849(A;A)
Reference rs81002849(G;G)
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.32900635G>A
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044588.2, RCV000113730.1, RCV000131857.2,