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rs397507947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507947(-;-)
Make rs397507947(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363177
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507947
ebirs397507947
HLIrs397507947
Exacrs397507947
Varsomers397507947
Maprs397507947
PheGenIrs397507947
hapmaprs397507947
1000 genomesrs397507947
hgdprs397507947
ensemblrs397507947
gopubmedrs397507947
geneviewrs397507947
scholarrs397507947
googlers397507947
pharmgkbrs397507947
gwascentralrs397507947
openSNPrs397507947
23andMers397507947
23andMe allrs397507947
SNP Nexus

SNPshotrs397507947
SNPdbers397507947
MSV3drs397507947
GWAS Ctlgrs397507947
Max Magnitude0
ClinVar
Risk rs397507947(;)
Alt rs397507947(;)
Reference rs397507947(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.32937314delA
CLNSRC ClinVar
CLNACC RCV000045369.2,