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rs786204821

From SNPedia

Orientationminus
Geno Mag Summary
(CTTT;CTTT) 0 common in clinvar
Make rs786204821(-;-)
Make rs786204821(-;CTTT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144399007
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204821
ebirs786204821
HLIrs786204821
Exacrs786204821
Varsomers786204821
Maprs786204821
PheGenIrs786204821
hapmaprs786204821
1000 genomesrs786204821
hgdprs786204821
ensemblrs786204821
gopubmedrs786204821
geneviewrs786204821
scholarrs786204821
googlers786204821
pharmgkbrs786204821
gwascentralrs786204821
openSNPrs786204821
23andMers786204821
23andMe allrs786204821
SNP Nexus

SNPshotrs786204821
SNPdbers786204821
MSV3drs786204821
GWAS Ctlgrs786204821
Max Magnitude0
ClinVar
Risk rs786204821(;)
Alt rs786204821(;)
Reference rs786204821(CTTT;CTTT)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156574_145156577delAAAG
CLNSRC
CLNACC RCV000169722.1,