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rs81002893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002893(A;G)
Make rs81002893(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376795
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002893
ebirs81002893
HLIrs81002893
Exacrs81002893
Varsomers81002893
Maprs81002893
PheGenIrs81002893
hapmaprs81002893
1000 genomesrs81002893
hgdprs81002893
ensemblrs81002893
gopubmedrs81002893
geneviewrs81002893
scholarrs81002893
googlers81002893
pharmgkbrs81002893
gwascentralrs81002893
openSNPrs81002893
23andMers81002893
23andMe allrs81002893
SNP Nexus

SNPshotrs81002893
SNPdbers81002893
MSV3drs81002893
GWAS Ctlgrs81002893
Max Magnitude0
ClinVar
Risk rs81002893(G;G)
Alt rs81002893(G;G)
Reference rs81002893(A;A)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32950932A>G; NC_000013.10:g.32950932A>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045615.2, RCV000077450.5, RCV000204178.1,