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rs397515732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515732(-;-)
Make rs397515732(-;A)
Make rs397515732(A;A)
ReferenceGRCh38 38.1/141
Chromosome5
Position112835124
GeneAPC
is asnp
is mentioned by
dbSNPrs397515732
ebirs397515732
HLIrs397515732
Exacrs397515732
Varsomers397515732
Maprs397515732
PheGenIrs397515732
hapmaprs397515732
1000 genomesrs397515732
hgdprs397515732
ensemblrs397515732
gopubmedrs397515732
geneviewrs397515732
scholarrs397515732
googlers397515732
pharmgkbrs397515732
gwascentralrs397515732
openSNPrs397515732
23andMers397515732
23andMe allrs397515732
SNP Nexus

SNPshotrs397515732
SNPdbers397515732
MSV3drs397515732
GWAS Ctlgrs397515732
Max Magnitude0
ClinVar
Risk rs397515732(A;A)
Alt rs397515732(A;A)
Reference rs397515732(;)
Significance Probable-Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112170821dupA
CLNSRC ClinVar
CLNACC RCV000035067.2,