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rs81002899

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs81002899(G;G)
Make rs81002899(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32326615
GeneBRCA2
is asnp
is mentioned by
dbSNPrs81002899
ebirs81002899
HLIrs81002899
Exacrs81002899
Varsomers81002899
Maprs81002899
PheGenIrs81002899
hapmaprs81002899
1000 genomesrs81002899
hgdprs81002899
ensemblrs81002899
gopubmedrs81002899
geneviewrs81002899
scholarrs81002899
googlers81002899
pharmgkbrs81002899
gwascentralrs81002899
openSNPrs81002899
23andMers81002899
23andMe allrs81002899
SNP Nexus

SNPshotrs81002899
SNPdbers81002899
MSV3drs81002899
GWAS Ctlgrs81002899
Max Magnitude0
ClinVar
Risk rs81002899(C,G;C,G)
Alt rs81002899(C,G;C,G)
Reference rs81002899(T;T)
Significance Pathogenic
Disease Familial cancer of breast Fanconi anemia Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Fanconi anemia, complementation group D1 Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32900752T>C; NC_000013.10:g.32900752T>G
CLNSRC Breast Cancer Information Core (BRCA2) OMIM Allelic Variant
CLNACC RCV000044896.2, RCV000009943.3, RCV000031615.5, RCV000044897.4, RCV000129071.2, RCV000195357.2,