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rs730881206

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881206(C;T)
Make rs730881206(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144517292
GeneZEB2
is asnp
is mentioned by
dbSNPrs730881206
ebirs730881206
HLIrs730881206
Exacrs730881206
Varsomers730881206
Maprs730881206
PheGenIrs730881206
hapmaprs730881206
1000 genomesrs730881206
hgdprs730881206
ensemblrs730881206
gopubmedrs730881206
geneviewrs730881206
scholarrs730881206
googlers730881206
pharmgkbrs730881206
gwascentralrs730881206
openSNPrs730881206
23andMers730881206
23andMe allrs730881206
SNP Nexus

SNPshotrs730881206
SNPdbers730881206
MSV3drs730881206
GWAS Ctlgrs730881206
Max Magnitude0
ClinVar
Risk rs730881206(T;T)
Alt rs730881206(T;T)
Reference rs730881206(C;C)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145274859G>A
CLNSRC
CLNACC RCV000159489.1,