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rs786204811

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204811(-;-)
Make rs786204811(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399303
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204811
ebirs786204811
HLIrs786204811
Exacrs786204811
Varsomers786204811
Maprs786204811
PheGenIrs786204811
hapmaprs786204811
1000 genomesrs786204811
hgdprs786204811
ensemblrs786204811
gopubmedrs786204811
geneviewrs786204811
scholarrs786204811
googlers786204811
pharmgkbrs786204811
gwascentralrs786204811
openSNPrs786204811
23andMers786204811
23andMe allrs786204811
SNP Nexus

SNPshotrs786204811
SNPdbers786204811
MSV3drs786204811
GWAS Ctlgrs786204811
Max Magnitude0
ClinVar
Risk rs786204811(;)
Alt rs786204811(;)
Reference rs786204811(T;T)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156870delA
CLNSRC
CLNACC RCV000169710.1,