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rs397507882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507882(A;A)
Make rs397507882(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32319061
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507882
ebirs397507882
HLIrs397507882
Exacrs397507882
Varsomers397507882
Maprs397507882
PheGenIrs397507882
hapmaprs397507882
1000 genomesrs397507882
hgdprs397507882
ensemblrs397507882
gopubmedrs397507882
geneviewrs397507882
scholarrs397507882
googlers397507882
pharmgkbrs397507882
gwascentralrs397507882
openSNPrs397507882
23andMers397507882
23andMe allrs397507882
SNP Nexus

SNPshotrs397507882
SNPdbers397507882
MSV3drs397507882
GWAS Ctlgrs397507882
Max Magnitude0
ClinVar
Risk rs397507882(A;A)
Alt rs397507882(A;A)
Reference rs397507882(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32893198T>A
CLNSRC ClinVar
CLNACC RCV000045050.2,