Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852981

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852981(C;T)
Make rs137852981(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position144399104
GeneZEB2
is asnp
is mentioned by
dbSNPrs137852981
ebirs137852981
HLIrs137852981
Exacrs137852981
Varsomers137852981
Maprs137852981
PheGenIrs137852981
hapmaprs137852981
1000 genomesrs137852981
hgdprs137852981
ensemblrs137852981
gopubmedrs137852981
geneviewrs137852981
scholarrs137852981
googlers137852981
pharmgkbrs137852981
gwascentralrs137852981
openSNPrs137852981
23andMers137852981
23andMe allrs137852981
SNP Nexus

SNPshotrs137852981
SNPdbers137852981
MSV3drs137852981
GWAS Ctlgrs137852981
Max Magnitude0
OMIM605802
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852981(T;T)
Alt rs137852981(T;T)
Reference rs137852981(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome not provided
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome not provided
Reversed 1
HGVS NC_000002.11:g.145156671G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000005021.9, RCV000213082.1,