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rs398123121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123121(C;T)
Make rs398123121(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112839576
GeneAPC
is asnp
is mentioned by
dbSNPrs398123121
ebirs398123121
HLIrs398123121
Exacrs398123121
Varsomers398123121
Maprs398123121
PheGenIrs398123121
hapmaprs398123121
1000 genomesrs398123121
hgdprs398123121
ensemblrs398123121
gopubmedrs398123121
geneviewrs398123121
scholarrs398123121
googlers398123121
pharmgkbrs398123121
gwascentralrs398123121
openSNPrs398123121
23andMers398123121
23andMe allrs398123121
SNP Nexus

SNPshotrs398123121
SNPdbers398123121
MSV3drs398123121
GWAS Ctlgrs398123121
Max Magnitude0
ClinVar
Risk rs398123121(T;T)
Alt rs398123121(T;T)
Reference rs398123121(C;C)
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.112175273C>T
CLNSRC HGMD
CLNACC RCV000077990.3, RCV000174982.1,