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rs786204809

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204809(-;-)
Make rs786204809(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399433
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204809
ebirs786204809
HLIrs786204809
Exacrs786204809
Varsomers786204809
Maprs786204809
PheGenIrs786204809
hapmaprs786204809
1000 genomesrs786204809
hgdprs786204809
ensemblrs786204809
gopubmedrs786204809
geneviewrs786204809
scholarrs786204809
googlers786204809
pharmgkbrs786204809
gwascentralrs786204809
openSNPrs786204809
23andMers786204809
23andMe allrs786204809
SNP Nexus

SNPshotrs786204809
SNPdbers786204809
MSV3drs786204809
GWAS Ctlgrs786204809
Max Magnitude0
ClinVar
Risk rs786204809(;)
Alt rs786204809(;)
Reference rs786204809(T;T)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157000delA
CLNSRC
CLNACC RCV000169708.1,