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rs786204817

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204817(-;-)
Make rs786204817(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144404968
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204817
ebirs786204817
HLIrs786204817
Exacrs786204817
Varsomers786204817
Maprs786204817
PheGenIrs786204817
hapmaprs786204817
1000 genomesrs786204817
hgdprs786204817
ensemblrs786204817
gopubmedrs786204817
geneviewrs786204817
scholarrs786204817
googlers786204817
pharmgkbrs786204817
gwascentralrs786204817
openSNPrs786204817
23andMers786204817
23andMe allrs786204817
SNP Nexus

SNPshotrs786204817
SNPdbers786204817
MSV3drs786204817
GWAS Ctlgrs786204817
Max Magnitude0
ClinVar
Risk rs786204817(;)
Alt rs786204817(;)
Reference rs786204817(G;G)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145162535delC
CLNSRC
CLNACC RCV000169717.1,