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rs587776606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776606(-;-)
Make rs587776606(-;A)
Make rs587776606(A;A)
ReferenceGRCh38 38.1/142
Chromosome2
Position144398734
GeneZEB2
is asnp
is mentioned by
dbSNPrs587776606
ebirs587776606
HLIrs587776606
Exacrs587776606
Varsomers587776606
Maprs587776606
PheGenIrs587776606
hapmaprs587776606
1000 genomesrs587776606
hgdprs587776606
ensemblrs587776606
gopubmedrs587776606
geneviewrs587776606
scholarrs587776606
googlers587776606
pharmgkbrs587776606
gwascentralrs587776606
openSNPrs587776606
23andMers587776606
23andMe allrs587776606
SNP Nexus

SNPshotrs587776606
SNPdbers587776606
MSV3drs587776606
GWAS Ctlgrs587776606
Max Magnitude0
ClinVar
Risk rs587776606(A;A)
Alt rs587776606(A;A)
Reference rs587776606(;)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 0
HGVS NC_000002.11:g.145156301dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005025.2,