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rs397507581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507581(G;T)
Make rs397507581(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319142
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507581
ebirs397507581
HLIrs397507581
Exacrs397507581
Varsomers397507581
Maprs397507581
PheGenIrs397507581
hapmaprs397507581
1000 genomesrs397507581
hgdprs397507581
ensemblrs397507581
gopubmedrs397507581
geneviewrs397507581
scholarrs397507581
googlers397507581
pharmgkbrs397507581
gwascentralrs397507581
openSNPrs397507581
23andMers397507581
23andMe allrs397507581
SNP Nexus

SNPshotrs397507581
SNPdbers397507581
MSV3drs397507581
GWAS Ctlgrs397507581
Max Magnitude0
ClinVar
Risk rs397507581(T;T)
Alt rs397507581(T;T)
Reference rs397507581(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893279G>T
CLNSRC ClinVar
CLNACC RCV000043784.2,