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rs398123117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123117(C;T)
Make rs398123117(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112837959
GeneAPC
is asnp
is mentioned by
dbSNPrs398123117
ebirs398123117
HLIrs398123117
Exacrs398123117
Varsomers398123117
Maprs398123117
PheGenIrs398123117
hapmaprs398123117
1000 genomesrs398123117
hgdprs398123117
ensemblrs398123117
gopubmedrs398123117
geneviewrs398123117
scholarrs398123117
googlers398123117
pharmgkbrs398123117
gwascentralrs398123117
openSNPrs398123117
23andMers398123117
23andMe allrs398123117
SNP Nexus

SNPshotrs398123117
SNPdbers398123117
MSV3drs398123117
GWAS Ctlgrs398123117
Max Magnitude0
ClinVar
Risk rs398123117(T;T)
Alt rs398123117(T;T)
Reference rs398123117(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.112173656C>T
CLNSRC HGMD
CLNACC RCV000077983.3, RCV000174978.1,