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rs786204810

From SNPedia

Orientationminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs786204810(-;-)
Make rs786204810(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399007
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204810
ebirs786204810
HLIrs786204810
Exacrs786204810
Varsomers786204810
Maprs786204810
PheGenIrs786204810
hapmaprs786204810
1000 genomesrs786204810
hgdprs786204810
ensemblrs786204810
gopubmedrs786204810
geneviewrs786204810
scholarrs786204810
googlers786204810
pharmgkbrs786204810
gwascentralrs786204810
openSNPrs786204810
23andMers786204810
23andMe allrs786204810
SNP Nexus

SNPshotrs786204810
SNPdbers786204810
MSV3drs786204810
GWAS Ctlgrs786204810
Max Magnitude0
ClinVar
Risk rs786204810(;)
Alt rs786204810(;)
Reference rs786204810(TT;TT)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156574_145156575delAA
CLNSRC
CLNACC RCV000169709.1,