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rs397507589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGT;AGT) 0 common in clinvar
Make rs397507589(AGT;TTAC)
Make rs397507589(TTAC;TTAC)
ReferenceGRCh38 38.1/141
Chromosome13
Position32332927
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507589
ebirs397507589
HLIrs397507589
Exacrs397507589
Varsomers397507589
Maprs397507589
PheGenIrs397507589
hapmaprs397507589
1000 genomesrs397507589
hgdprs397507589
ensemblrs397507589
gopubmedrs397507589
geneviewrs397507589
scholarrs397507589
googlers397507589
pharmgkbrs397507589
gwascentralrs397507589
openSNPrs397507589
23andMers397507589
23andMe allrs397507589
SNP Nexus

SNPshotrs397507589
SNPdbers397507589
MSV3drs397507589
GWAS Ctlgrs397507589
Max Magnitude0
ClinVar
Risk rs397507589(TTAC;TTAC)
Alt rs397507589(TTAC;TTAC)
Reference rs397507589(AGT;AGT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907064_32907066delAGTinsTTAC
CLNSRC ClinVar
CLNACC RCV000043809.2,