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rs786204807

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204807(G;G)
Make rs786204807(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399910
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204807
ebirs786204807
HLIrs786204807
Exacrs786204807
Varsomers786204807
Maprs786204807
PheGenIrs786204807
hapmaprs786204807
1000 genomesrs786204807
hgdprs786204807
ensemblrs786204807
gopubmedrs786204807
geneviewrs786204807
scholarrs786204807
googlers786204807
pharmgkbrs786204807
gwascentralrs786204807
openSNPrs786204807
23andMers786204807
23andMe allrs786204807
SNP Nexus

SNPshotrs786204807
SNPdbers786204807
MSV3drs786204807
GWAS Ctlgrs786204807
Max Magnitude0
ClinVar
Risk rs786204807(G;G)
Alt rs786204807(G;G)
Reference rs786204807(T;T)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157477A>C
CLNSRC
CLNACC RCV000169706.1,