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rs397507876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507876(-;-)
Make rs397507876(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341039
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507876
ebirs397507876
HLIrs397507876
Exacrs397507876
Varsomers397507876
Maprs397507876
PheGenIrs397507876
hapmaprs397507876
1000 genomesrs397507876
hgdprs397507876
ensemblrs397507876
gopubmedrs397507876
geneviewrs397507876
scholarrs397507876
googlers397507876
pharmgkbrs397507876
gwascentralrs397507876
openSNPrs397507876
23andMers397507876
23andMe allrs397507876
SNP Nexus

SNPshotrs397507876
SNPdbers397507876
MSV3drs397507876
GWAS Ctlgrs397507876
Max Magnitude0
ClinVar
Risk rs397507876(;)
Alt rs397507876(;)
Reference rs397507876(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32915176delA
CLNSRC ClinVar
CLNACC RCV000045018.2,