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rs81002823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs81002823(A;T)
Make rs81002823(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32354859
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002823
ebirs81002823
HLIrs81002823
Exacrs81002823
Varsomers81002823
Maprs81002823
PheGenIrs81002823
hapmaprs81002823
1000 genomesrs81002823
hgdprs81002823
ensemblrs81002823
gopubmedrs81002823
geneviewrs81002823
scholarrs81002823
googlers81002823
pharmgkbrs81002823
gwascentralrs81002823
openSNPrs81002823
23andMers81002823
23andMe allrs81002823
SNP Nexus

SNPshotrs81002823
SNPdbers81002823
MSV3drs81002823
GWAS Ctlgrs81002823
Max Magnitude0
ClinVar
Risk rs81002823(G,T;G,T)
Alt rs81002823(G,T;G,T)
Reference rs81002823(A;A)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000013.10:g.32928996A>G; NC_000013.10:g.32928996A>T
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000045117.2, RCV000113688.1, RCV000045118.2, RCV000113689.2, RCV000220759.1, RCV000235662.1,