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rs786204819

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204819(-;-)
Make rs786204819(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399500
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204819
ebirs786204819
HLIrs786204819
Exacrs786204819
Varsomers786204819
Maprs786204819
PheGenIrs786204819
hapmaprs786204819
1000 genomesrs786204819
hgdprs786204819
ensemblrs786204819
gopubmedrs786204819
geneviewrs786204819
scholarrs786204819
googlers786204819
pharmgkbrs786204819
gwascentralrs786204819
openSNPrs786204819
23andMers786204819
23andMe allrs786204819
SNP Nexus

SNPshotrs786204819
SNPdbers786204819
MSV3drs786204819
GWAS Ctlgrs786204819
Max Magnitude0
ClinVar
Risk rs786204819(;)
Alt rs786204819(;)
Reference rs786204819(A;A)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157067delT
CLNSRC
CLNACC RCV000169720.1,