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rs398123119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123119(G;T)
Make rs398123119(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112838325
GeneAPC
is asnp
is mentioned by
dbSNPrs398123119
ebirs398123119
HLIrs398123119
Exacrs398123119
Varsomers398123119
Maprs398123119
PheGenIrs398123119
hapmaprs398123119
1000 genomesrs398123119
hgdprs398123119
ensemblrs398123119
gopubmedrs398123119
geneviewrs398123119
scholarrs398123119
googlers398123119
pharmgkbrs398123119
gwascentralrs398123119
openSNPrs398123119
23andMers398123119
23andMe allrs398123119
SNP Nexus

SNPshotrs398123119
SNPdbers398123119
MSV3drs398123119
GWAS Ctlgrs398123119
Max Magnitude0
ClinVar
Risk rs398123119(T;T)
Alt rs398123119(T;T)
Reference rs398123119(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.112174022G>T
CLNSRC ClinVar Emory University
CLNACC RCV000077985.3, RCV000174980.1,