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rs81002795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002795(A;T)
Make rs81002795(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326153
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002795
ebirs81002795
HLIrs81002795
Exacrs81002795
Varsomers81002795
Maprs81002795
PheGenIrs81002795
hapmaprs81002795
1000 genomesrs81002795
hgdprs81002795
ensemblrs81002795
gopubmedrs81002795
geneviewrs81002795
scholarrs81002795
googlers81002795
pharmgkbrs81002795
gwascentralrs81002795
openSNPrs81002795
23andMers81002795
23andMe allrs81002795
SNP Nexus

SNPshotrs81002795
SNPdbers81002795
MSV3drs81002795
GWAS Ctlgrs81002795
Max Magnitude0
ClinVar
Risk rs81002795(G,T;G,T)
Alt rs81002795(G,T;G,T)
Reference rs81002795(A;A)
Significance Untested
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.32900290A>G; NC_000013.10:g.32900290A>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000044484.2, RCV000113646.1,