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rs730881216

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881216(A;A)
Make rs730881216(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144390010
GeneZEB2
is asnp
is mentioned by
dbSNPrs730881216
ClinGenrs730881216
ebirs730881216
HLIrs730881216
Exacrs730881216
Varsomers730881216
Maprs730881216
PheGenIrs730881216
hapmaprs730881216
1000 genomesrs730881216
hgdprs730881216
ensemblrs730881216
gopubmedrs730881216
geneviewrs730881216
scholarrs730881216
googlers730881216
pharmgkbrs730881216
gwascentralrs730881216
openSNPrs730881216
23andMers730881216
23andMe allrs730881216
SNP Nexus

SNPshotrs730881216
SNPdbers730881216
MSV3drs730881216
GWAS Ctlgrs730881216
Max Magnitude0
ClinVar
Risk rs730881216(A;A)
Alt rs730881216(A;A)
Reference Rs730881216(G;G)
Significance Probable-Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 1
HGVS NC_000002.11:g.145147577C>T
CLNSRC
CLNACC RCV000159500.1,