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

rs786204814

From SNPedia

Orientationminus
Geno Mag Summary
(CAGGC;CAGGC) 0 common in clinvar
Make rs786204814(-;-)
Make rs786204814(-;CAGGC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399767
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204814
ebirs786204814
HLIrs786204814
Exacrs786204814
Varsomers786204814
Maprs786204814
PheGenIrs786204814
hapmaprs786204814
1000 genomesrs786204814
hgdprs786204814
ensemblrs786204814
gopubmedrs786204814
geneviewrs786204814
scholarrs786204814
googlers786204814
pharmgkbrs786204814
gwascentralrs786204814
openSNPrs786204814
23andMers786204814
23andMe allrs786204814
SNP Nexus

SNPshotrs786204814
SNPdbers786204814
MSV3drs786204814
GWAS Ctlgrs786204814
Max Magnitude0
ClinVar
Risk rs786204814(;)
Alt rs786204814(;)
Reference rs786204814(CAGGC;CAGGC)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157334_145157338delGCCTG
CLNSRC
CLNACC RCV000169714.1,