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rs398124276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124276(-;-)
Make rs398124276(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position144399601
GeneZEB2
is asnp
is mentioned by
dbSNPrs398124276
ebirs398124276
HLIrs398124276
Exacrs398124276
Varsomers398124276
Maprs398124276
PheGenIrs398124276
hapmaprs398124276
1000 genomesrs398124276
hgdprs398124276
ensemblrs398124276
gopubmedrs398124276
geneviewrs398124276
scholarrs398124276
googlers398124276
pharmgkbrs398124276
gwascentralrs398124276
openSNPrs398124276
23andMers398124276
23andMe allrs398124276
SNP Nexus

SNPshotrs398124276
SNPdbers398124276
MSV3drs398124276
GWAS Ctlgrs398124276
Max Magnitude0
ClinVar
Risk rs398124276(;)
Alt rs398124276(;)
Reference rs398124276(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157168delG
CLNSRC ClinVar
CLNACC RCV000081657.4,