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rs587784563

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784563(C;T)
Make rs587784563(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144399231
GeneZEB2
is asnp
is mentioned by
dbSNPrs587784563
ebirs587784563
HLIrs587784563
Exacrs587784563
Varsomers587784563
Maprs587784563
PheGenIrs587784563
hapmaprs587784563
1000 genomesrs587784563
hgdprs587784563
ensemblrs587784563
gopubmedrs587784563
geneviewrs587784563
scholarrs587784563
googlers587784563
pharmgkbrs587784563
gwascentralrs587784563
openSNPrs587784563
23andMers587784563
23andMe allrs587784563
SNP Nexus

SNPshotrs587784563
SNPdbers587784563
MSV3drs587784563
GWAS Ctlgrs587784563
Max Magnitude0
ClinVar
Risk rs587784563(T;T)
Alt rs587784563(T;T)
Reference rs587784563(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156798G>A
CLNSRC
CLNACC RCV000147993.1,