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rs397514030

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs397514030(-;-)
Make rs397514030(-;AAG)
ReferenceGRCh38 38.1/141
Chromosome5
Position112819343
GeneAPC
is asnp
is mentioned by
dbSNPrs397514030
ebirs397514030
HLIrs397514030
Exacrs397514030
Varsomers397514030
Maprs397514030
PheGenIrs397514030
hapmaprs397514030
1000 genomesrs397514030
hgdprs397514030
ensemblrs397514030
gopubmedrs397514030
geneviewrs397514030
scholarrs397514030
googlers397514030
pharmgkbrs397514030
gwascentralrs397514030
openSNPrs397514030
23andMers397514030
23andMe allrs397514030
SNP Nexus

SNPshotrs397514030
SNPdbers397514030
MSV3drs397514030
GWAS Ctlgrs397514030
Max Magnitude0
ClinVar
Risk rs397514030(;)
Alt rs397514030(;)
Reference rs397514030(AAG;AAG)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112155040_112155042delAAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000869.2,