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rs587776609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776609(-;-)
Make rs587776609(-;GG)
Make rs587776609(GG;GG)
ReferenceGRCh38 38.1/142
Chromosome2
Position144389530
GeneZEB2
is asnp
is mentioned by
dbSNPrs587776609
ebirs587776609
HLIrs587776609
Exacrs587776609
Varsomers587776609
Maprs587776609
PheGenIrs587776609
hapmaprs587776609
1000 genomesrs587776609
hgdprs587776609
ensemblrs587776609
gopubmedrs587776609
geneviewrs587776609
scholarrs587776609
googlers587776609
pharmgkbrs587776609
gwascentralrs587776609
openSNPrs587776609
23andMers587776609
23andMe allrs587776609
SNP Nexus

SNPshotrs587776609
SNPdbers587776609
MSV3drs587776609
GWAS Ctlgrs587776609
Max Magnitude0
ClinVar
Risk rs587776609(GG;GG)
Alt rs587776609(GG;GG)
Reference rs587776609(;)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 0
HGVS NC_000002.11:g.145147096_145147097dupGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000005029.2,