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rs587784566

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784566(C;T)
Make rs587784566(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144398426
GeneZEB2
is asnp
is mentioned by
dbSNPrs587784566
ebirs587784566
HLIrs587784566
Exacrs587784566
Varsomers587784566
Maprs587784566
PheGenIrs587784566
hapmaprs587784566
1000 genomesrs587784566
hgdprs587784566
ensemblrs587784566
gopubmedrs587784566
geneviewrs587784566
scholarrs587784566
googlers587784566
pharmgkbrs587784566
gwascentralrs587784566
openSNPrs587784566
23andMers587784566
23andMe allrs587784566
SNP Nexus

SNPshotrs587784566
SNPdbers587784566
MSV3drs587784566
GWAS Ctlgrs587784566
Max Magnitude0
ClinVar
Risk rs587784566(T;T)
Alt rs587784566(T;T)
Reference rs587784566(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.145155993G>A
CLNSRC
CLNACC RCV000147998.3, RCV000213083.1,