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rs398123122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123122(-;-)
Make rs398123122(-;T)
Make rs398123122(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112840067
GeneAPC
is asnp
is mentioned by
dbSNPrs398123122
ebirs398123122
HLIrs398123122
Exacrs398123122
Varsomers398123122
Maprs398123122
PheGenIrs398123122
hapmaprs398123122
1000 genomesrs398123122
hgdprs398123122
ensemblrs398123122
gopubmedrs398123122
geneviewrs398123122
scholarrs398123122
googlers398123122
pharmgkbrs398123122
gwascentralrs398123122
openSNPrs398123122
23andMers398123122
23andMe allrs398123122
SNP Nexus

SNPshotrs398123122
SNPdbers398123122
MSV3drs398123122
GWAS Ctlgrs398123122
Max Magnitude0
ClinVar
Risk rs398123122(T;T)
Alt rs398123122(T;T)
Reference rs398123122(;)
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.112175764dupT
CLNSRC ClinVar
CLNACC RCV000077991.3, RCV000174979.1,