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

rs587776607

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776607(-;-)
Make rs587776607(-;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position144399295
GeneZEB2
is asnp
is mentioned by
dbSNPrs587776607
dbSNP (classic)rs587776607
ClinGenrs587776607
ebirs587776607
HLIrs587776607
Exacrs587776607
Gnomadrs587776607
Varsomers587776607
LitVarrs587776607
Maprs587776607
PheGenIrs587776607
Biobankrs587776607
1000 genomesrs587776607
hgdprs587776607
ensemblrs587776607
geneviewrs587776607
scholarrs587776607
googlers587776607
pharmgkbrs587776607
gwascentralrs587776607
openSNPrs587776607
23andMers587776607
SNPshotrs587776607
SNPdbers587776607
MSV3drs587776607
GWAS Ctlgrs587776607
Max Magnitude0
ClinVar
Risk Rs587776607(T;T) rs587776607(-;-)
Alt Rs587776607(T;T) rs587776607(-;-)
Reference Rs587776607(A;A)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156862delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000005026.2,