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rs398124282

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124282(C;C)
Make rs398124282(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position144517276
GeneZEB2
is asnp
is mentioned by
dbSNPrs398124282
ebirs398124282
HLIrs398124282
Exacrs398124282
Varsomers398124282
Maprs398124282
PheGenIrs398124282
hapmaprs398124282
1000 genomesrs398124282
hgdprs398124282
ensemblrs398124282
gopubmedrs398124282
geneviewrs398124282
scholarrs398124282
googlers398124282
pharmgkbrs398124282
gwascentralrs398124282
openSNPrs398124282
23andMers398124282
23andMe allrs398124282
SNP Nexus

SNPshotrs398124282
SNPdbers398124282
MSV3drs398124282
GWAS Ctlgrs398124282
Max Magnitude0
ClinVar
Risk rs398124282(C;C)
Alt rs398124282(C;C)
Reference rs398124282(T;T)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145274843A>G
CLNSRC ClinVar
CLNACC RCV000081673.4,