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rs797046122

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797046122(A;A)
Make rs797046122(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144404049
GeneZEB2
is asnp
is mentioned by
dbSNPrs797046122
ebirs797046122
HLIrs797046122
Exacrs797046122
Varsomers797046122
Maprs797046122
PheGenIrs797046122
hapmaprs797046122
1000 genomesrs797046122
hgdprs797046122
ensemblrs797046122
gopubmedrs797046122
geneviewrs797046122
scholarrs797046122
googlers797046122
pharmgkbrs797046122
gwascentralrs797046122
openSNPrs797046122
23andMers797046122
23andMe allrs797046122
SNP Nexus

SNPshotrs797046122
SNPdbers797046122
MSV3drs797046122
GWAS Ctlgrs797046122
Max Magnitude0
ClinVar
Risk rs797046122(A;A)
Alt rs797046122(A;A)
Reference rs797046122(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145161616G>T
CLNSRC
CLNACC RCV000192869.1,