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rs137852980

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852980(A;T)
Make rs137852980(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position144399542
GeneZEB2
is asnp
is mentioned by
dbSNPrs137852980
ebirs137852980
HLIrs137852980
Exacrs137852980
Varsomers137852980
Maprs137852980
PheGenIrs137852980
hapmaprs137852980
1000 genomesrs137852980
hgdprs137852980
ensemblrs137852980
gopubmedrs137852980
geneviewrs137852980
scholarrs137852980
googlers137852980
pharmgkbrs137852980
gwascentralrs137852980
openSNPrs137852980
23andMers137852980
23andMe allrs137852980
SNP Nexus

SNPshotrs137852980
SNPdbers137852980
MSV3drs137852980
GWAS Ctlgrs137852980
Max Magnitude0
OMIM605802
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852980(T;T)
Alt rs137852980(T;T)
Reference rs137852980(A;A)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157109T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005020.2,