Have questions? Visit https://www.reddit.com/r/SNPedia

rs587784570

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784570(C;T)
Make rs587784570(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144401292
GeneZEB2
is asnp
is mentioned by
dbSNPrs587784570
ebirs587784570
HLIrs587784570
Exacrs587784570
Varsomers587784570
Maprs587784570
PheGenIrs587784570
hapmaprs587784570
1000 genomesrs587784570
hgdprs587784570
ensemblrs587784570
gopubmedrs587784570
geneviewrs587784570
scholarrs587784570
googlers587784570
pharmgkbrs587784570
gwascentralrs587784570
openSNPrs587784570
23andMers587784570
23andMe allrs587784570
SNP Nexus

SNPshotrs587784570
SNPdbers587784570
MSV3drs587784570
GWAS Ctlgrs587784570
Max Magnitude0
ClinVar
Risk rs587784570(G,T;G,T)
Alt rs587784570(G,T;G,T)
Reference rs587784570(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145158859G>A
CLNSRC
CLNACC RCV000148006.1,