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rs398123116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123116(A;A)
Make rs398123116(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position112828888
GeneAPC
is asnp
is mentioned by
dbSNPrs398123116
dbSNP (classic)rs398123116
ClinGenrs398123116
ebirs398123116
HLIrs398123116
Exacrs398123116
Gnomadrs398123116
Varsomers398123116
LitVarrs398123116
Maprs398123116
PheGenIrs398123116
Biobankrs398123116
1000 genomesrs398123116
hgdprs398123116
ensemblrs398123116
geneviewrs398123116
scholarrs398123116
googlers398123116
pharmgkbrs398123116
gwascentralrs398123116
openSNPrs398123116
23andMers398123116
SNPshotrs398123116
SNPdbers398123116
MSV3drs398123116
GWAS Ctlgrs398123116
Max Magnitude0
ClinVar
Risk rs398123116(A;A)
Alt rs398123116(A;A)
Reference Rs398123116(G;G)
Significance Pathogenic
Disease not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112164585G>A
CLNSRC ClinVar Emory University
CLNACC RCV000077981.3, RCV000174655.1,