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rs756686919

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756686919(C;C)
Make rs756686919(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position144400207
GeneZEB2
is asnp
is mentioned by
dbSNPrs756686919
ebirs756686919
HLIrs756686919
Exacrs756686919
Varsomers756686919
Maprs756686919
PheGenIrs756686919
hapmaprs756686919
1000 genomesrs756686919
hgdprs756686919
ensemblrs756686919
gopubmedrs756686919
geneviewrs756686919
scholarrs756686919
googlers756686919
pharmgkbrs756686919
gwascentralrs756686919
openSNPrs756686919
23andMers756686919
23andMe allrs756686919
SNP Nexus

SNPshotrs756686919
SNPdbers756686919
MSV3drs756686919
GWAS Ctlgrs756686919
Max Magnitude0
ClinVar
Risk rs756686919(C;C)
Alt rs756686919(C;C)
Reference rs756686919(G;G)
Significance Pathogenic
Disease Mowat-Wilson syndrome
Variation info
Gene ZEB2
CLNDBN Mowat-Wilson syndrome
Reversed 0
HGVS NC_000002.11:g.145157774G>T
CLNSRC
CLNACC RCV000180324.1,