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rs397507864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507864(-;-)
Make rs397507864(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340882
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507864
ebirs397507864
HLIrs397507864
Exacrs397507864
Varsomers397507864
Maprs397507864
PheGenIrs397507864
hapmaprs397507864
1000 genomesrs397507864
hgdprs397507864
ensemblrs397507864
gopubmedrs397507864
geneviewrs397507864
scholarrs397507864
googlers397507864
pharmgkbrs397507864
gwascentralrs397507864
openSNPrs397507864
23andMers397507864
23andMe allrs397507864
SNP Nexus

SNPshotrs397507864
SNPdbers397507864
MSV3drs397507864
GWAS Ctlgrs397507864
Max Magnitude0
ClinVar
Risk rs397507864(;)
Alt rs397507864(;)
Reference rs397507864(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.32915019delA
CLNSRC ClinVar
CLNACC RCV000044975.2,