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rs397507879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507879(-;-)
Make rs397507879(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32341087
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507879
ebirs397507879
HLIrs397507879
Exacrs397507879
Varsomers397507879
Maprs397507879
PheGenIrs397507879
hapmaprs397507879
1000 genomesrs397507879
hgdprs397507879
ensemblrs397507879
gopubmedrs397507879
geneviewrs397507879
scholarrs397507879
googlers397507879
pharmgkbrs397507879
gwascentralrs397507879
openSNPrs397507879
23andMers397507879
23andMe allrs397507879
SNP Nexus

SNPshotrs397507879
SNPdbers397507879
MSV3drs397507879
GWAS Ctlgrs397507879
Max Magnitude0
ClinVar
Risk rs397507879(;)
Alt rs397507879(;)
Reference rs397507879(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.32915224delA
CLNSRC ClinVar
CLNACC RCV000045033.2,