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rs397515734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515734(C;T)
Make rs397515734(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112792494
GeneAPC
is asnp
is mentioned by
dbSNPrs397515734
ebirs397515734
HLIrs397515734
Exacrs397515734
Varsomers397515734
Maprs397515734
PheGenIrs397515734
hapmaprs397515734
1000 genomesrs397515734
hgdprs397515734
ensemblrs397515734
gopubmedrs397515734
geneviewrs397515734
scholarrs397515734
googlers397515734
pharmgkbrs397515734
gwascentralrs397515734
openSNPrs397515734
23andMers397515734
23andMe allrs397515734
SNP Nexus

SNPshotrs397515734
SNPdbers397515734
MSV3drs397515734
GWAS Ctlgrs397515734
Max Magnitude0
ClinVar
Risk rs397515734(T;T)
Alt rs397515734(T;T)
Reference rs397515734(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.112128191C>T
CLNSRC ClinVar
CLNACC RCV000035081.2,