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

rs587784571

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784571(C;T)
Make rs587784571(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144401211
GeneZEB2
is asnp
is mentioned by
dbSNPrs587784571
ebirs587784571
HLIrs587784571
Exacrs587784571
Varsomers587784571
Maprs587784571
PheGenIrs587784571
hapmaprs587784571
1000 genomesrs587784571
hgdprs587784571
ensemblrs587784571
gopubmedrs587784571
geneviewrs587784571
scholarrs587784571
googlers587784571
pharmgkbrs587784571
gwascentralrs587784571
openSNPrs587784571
23andMers587784571
23andMe allrs587784571
SNP Nexus

SNPshotrs587784571
SNPdbers587784571
MSV3drs587784571
GWAS Ctlgrs587784571
Max Magnitude0
ClinVar
Risk rs587784571(T;T)
Alt rs587784571(T;T)
Reference rs587784571(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome not provided
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome not provided
Reversed 1
HGVS NC_000002.11:g.145158778G>A
CLNSRC The Children's Hospital of Philadelphia
CLNACC RCV000148007.4, RCV000167554.1,