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

rs786204813

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204813(-;-)
Make rs786204813(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144517277
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204813
ebirs786204813
HLIrs786204813
Exacrs786204813
Varsomers786204813
Maprs786204813
PheGenIrs786204813
hapmaprs786204813
1000 genomesrs786204813
hgdprs786204813
ensemblrs786204813
gopubmedrs786204813
geneviewrs786204813
scholarrs786204813
googlers786204813
pharmgkbrs786204813
gwascentralrs786204813
openSNPrs786204813
23andMers786204813
23andMe allrs786204813
SNP Nexus

SNPshotrs786204813
SNPdbers786204813
MSV3drs786204813
GWAS Ctlgrs786204813
Max Magnitude0
ClinVar
Risk rs786204813(;)
Alt rs786204813(;)
Reference rs786204813(G;G)
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.145274844delC
CLNSRC
CLNACC RCV000169713.1, RCV000224619.1,