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rs34961586

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs34961586(C;C)
Make rs34961586(C;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position144403925
GeneZEB2
is asnp
is mentioned by
dbSNPrs34961586
ebirs34961586
HLIrs34961586
Exacrs34961586
Varsomers34961586
Maprs34961586
PheGenIrs34961586
hapmaprs34961586
1000 genomesrs34961586
hgdprs34961586
ensemblrs34961586
gopubmedrs34961586
geneviewrs34961586
scholarrs34961586
googlers34961586
pharmgkbrs34961586
gwascentralrs34961586
openSNPrs34961586
23andMers34961586
23andMe allrs34961586
SNP Nexus

SNPshotrs34961586
SNPdbers34961586
MSV3drs34961586
GWAS Ctlgrs34961586
Max Magnitude0

[PMID 24576558] The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease


ClinVar
Risk rs34961586(C;C)
Alt rs34961586(C;C)
Reference rs34961586(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ZEB2
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.145161492C>G
CLNSRC ClinVar GeneDx University of Chicago
CLNACC RCV000148005.3,