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rs786204812

From SNPedia

Orientationminus
Geno Mag Summary
(AAGCTCT;AAGCTCT) 0 common in clinvar
Make rs786204812(-;-)
Make rs786204812(-;AAGCTCT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position144429867
GeneZEB2
is asnp
is mentioned by
dbSNPrs786204812
ebirs786204812
HLIrs786204812
Exacrs786204812
Varsomers786204812
Maprs786204812
PheGenIrs786204812
hapmaprs786204812
1000 genomesrs786204812
hgdprs786204812
ensemblrs786204812
gopubmedrs786204812
geneviewrs786204812
scholarrs786204812
googlers786204812
pharmgkbrs786204812
gwascentralrs786204812
openSNPrs786204812
23andMers786204812
23andMe allrs786204812
SNP Nexus

SNPshotrs786204812
SNPdbers786204812
MSV3drs786204812
GWAS Ctlgrs786204812
Max Magnitude0
ClinVar
Risk rs786204812(;)
Alt rs786204812(;)
Reference rs786204812(AAGCTCT;AAGCTCT)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145187434_145187440delAGAGCTT
CLNSRC
CLNACC RCV000169712.1,