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

rs587776611

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs587776611(-;-)
Make rs587776611(-;A)
ReferenceGRCh38 38.1/142
Chromosome2
Position144399325
GeneZEB2
is asnp
is mentioned by
dbSNPrs587776611
ebirs587776611
HLIrs587776611
Exacrs587776611
Varsomers587776611
Maprs587776611
PheGenIrs587776611
hapmaprs587776611
1000 genomesrs587776611
hgdprs587776611
ensemblrs587776611
gopubmedrs587776611
geneviewrs587776611
scholarrs587776611
googlers587776611
pharmgkbrs587776611
gwascentralrs587776611
openSNPrs587776611
23andMers587776611
23andMe allrs587776611
SNP Nexus

SNPshotrs587776611
SNPdbers587776611
MSV3drs587776611
GWAS Ctlgrs587776611
Max Magnitude0
ClinVar
Risk rs587776611(AC,C;AC,C)
Alt rs587776611(AC,C;AC,C)
Reference rs587776611(TC;TC)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156892delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005032.2,