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rs587776608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776608(-;-)
Make rs587776608(-;CA)
Make rs587776608(CA;CA)
ReferenceGRCh38 38.1/142
Chromosome2
Position144404874
GeneZEB2
is asnp
is mentioned by
dbSNPrs587776608
ebirs587776608
HLIrs587776608
Exacrs587776608
Varsomers587776608
Maprs587776608
PheGenIrs587776608
hapmaprs587776608
1000 genomesrs587776608
hgdprs587776608
ensemblrs587776608
gopubmedrs587776608
geneviewrs587776608
scholarrs587776608
googlers587776608
pharmgkbrs587776608
gwascentralrs587776608
openSNPrs587776608
23andMers587776608
23andMe allrs587776608
SNP Nexus

SNPshotrs587776608
SNPdbers587776608
MSV3drs587776608
GWAS Ctlgrs587776608
Max Magnitude0
ClinVar
Risk rs587776608(CA;CA)
Alt rs587776608(CA;CA)
Reference rs587776608(;)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145162441_145162442insCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005027.2,