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rs730881211

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs730881211(-;-)
Make rs730881211(-;CT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144398958
GeneZEB2
is asnp
is mentioned by
dbSNPrs730881211
ebirs730881211
HLIrs730881211
Exacrs730881211
Varsomers730881211
Maprs730881211
PheGenIrs730881211
hapmaprs730881211
1000 genomesrs730881211
hgdprs730881211
ensemblrs730881211
gopubmedrs730881211
geneviewrs730881211
scholarrs730881211
googlers730881211
pharmgkbrs730881211
gwascentralrs730881211
openSNPrs730881211
23andMers730881211
23andMe allrs730881211
SNP Nexus

SNPshotrs730881211
SNPdbers730881211
MSV3drs730881211
GWAS Ctlgrs730881211
Max Magnitude0
ClinVar
Risk rs730881211(;)
Alt rs730881211(;)
Reference rs730881211(CT;CT)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145156525_145156526delAG
CLNSRC
CLNACC RCV000159494.1,