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rs786204803

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204803(-;-)
Make rs786204803(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399243
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204803
ebirs786204803
HLIrs786204803
Exacrs786204803
Varsomers786204803
Maprs786204803
PheGenIrs786204803
hapmaprs786204803
1000 genomesrs786204803
hgdprs786204803
ensemblrs786204803
gopubmedrs786204803
geneviewrs786204803
scholarrs786204803
googlers786204803
pharmgkbrs786204803
gwascentralrs786204803
openSNPrs786204803
23andMers786204803
23andMe allrs786204803
SNP Nexus

SNPshotrs786204803
SNPdbers786204803
MSV3drs786204803
GWAS Ctlgrs786204803
Max Magnitude0
ClinVar
Risk rs786204803(;)
Alt rs786204803(;)
Reference rs786204803(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156810delG
CLNSRC
CLNACC RCV000169698.1,