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rs786204815

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204815(C;T)
Make rs786204815(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144400160
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204815
ebirs786204815
HLIrs786204815
Exacrs786204815
Varsomers786204815
Maprs786204815
PheGenIrs786204815
hapmaprs786204815
1000 genomesrs786204815
hgdprs786204815
ensemblrs786204815
gopubmedrs786204815
geneviewrs786204815
scholarrs786204815
googlers786204815
pharmgkbrs786204815
gwascentralrs786204815
openSNPrs786204815
23andMers786204815
23andMe allrs786204815
SNP Nexus

SNPshotrs786204815
SNPdbers786204815
MSV3drs786204815
GWAS Ctlgrs786204815
Max Magnitude0
ClinVar
Risk rs786204815(T;T)
Alt rs786204815(T;T)
Reference rs786204815(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157727G>A
CLNSRC
CLNACC RCV000169715.3,