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rs786204820

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204820(-;-)
Make rs786204820(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399534
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204820
ebirs786204820
HLIrs786204820
Exacrs786204820
Varsomers786204820
Maprs786204820
PheGenIrs786204820
hapmaprs786204820
1000 genomesrs786204820
hgdprs786204820
ensemblrs786204820
gopubmedrs786204820
geneviewrs786204820
scholarrs786204820
googlers786204820
pharmgkbrs786204820
gwascentralrs786204820
openSNPrs786204820
23andMers786204820
23andMe allrs786204820
SNP Nexus

SNPshotrs786204820
SNPdbers786204820
MSV3drs786204820
GWAS Ctlgrs786204820
Max Magnitude0
ClinVar
Risk rs786204820(;)
Alt rs786204820(;)
Reference rs786204820(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145157101delG
CLNSRC
CLNACC RCV000169721.1,