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rs397515733

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515733(-;-)
Make rs397515733(-;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position112838756
GeneAPC
is asnp
is mentioned by
dbSNPrs397515733
ebirs397515733
HLIrs397515733
Exacrs397515733
Varsomers397515733
Maprs397515733
PheGenIrs397515733
hapmaprs397515733
1000 genomesrs397515733
hgdprs397515733
ensemblrs397515733
gopubmedrs397515733
geneviewrs397515733
scholarrs397515733
googlers397515733
pharmgkbrs397515733
gwascentralrs397515733
openSNPrs397515733
23andMers397515733
23andMe allrs397515733
SNP Nexus

SNPshotrs397515733
SNPdbers397515733
MSV3drs397515733
GWAS Ctlgrs397515733
Max Magnitude0
ClinVar
Risk rs397515733(;)
Alt rs397515733(;)
Reference rs397515733(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112174453delC
CLNSRC ClinVar
CLNACC RCV000035070.2,