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rs398124277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124277(-;-)
Make rs398124277(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position144399155
GeneZEB2
is asnp
is mentioned by
dbSNPrs398124277
ebirs398124277
HLIrs398124277
Exacrs398124277
Varsomers398124277
Maprs398124277
PheGenIrs398124277
hapmaprs398124277
1000 genomesrs398124277
hgdprs398124277
ensemblrs398124277
gopubmedrs398124277
geneviewrs398124277
scholarrs398124277
googlers398124277
pharmgkbrs398124277
gwascentralrs398124277
openSNPrs398124277
23andMers398124277
23andMe allrs398124277
SNP Nexus

SNPshotrs398124277
SNPdbers398124277
MSV3drs398124277
GWAS Ctlgrs398124277
Max Magnitude0
ClinVar
Risk rs398124277(;)
Alt rs398124277(;)
Reference rs398124277(T;T)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156722delA
CLNSRC ClinVar
CLNACC RCV000081659.4,