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rs193922719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922719(A;T)
Make rs193922719(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position42323120
GeneSTAT3
is asnp
is mentioned by
dbSNPrs193922719
ebirs193922719
HLIrs193922719
Exacrs193922719
Varsomers193922719
Maprs193922719
PheGenIrs193922719
hapmaprs193922719
1000 genomesrs193922719
hgdprs193922719
ensemblrs193922719
gopubmedrs193922719
geneviewrs193922719
scholarrs193922719
googlers193922719
pharmgkbrs193922719
gwascentralrs193922719
openSNPrs193922719
23andMers193922719
23andMe allrs193922719
SNP Nexus

SNPshotrs193922719
SNPdbers193922719
MSV3drs193922719
GWAS Ctlgrs193922719
Max Magnitude0
ClinVar
Risk rs193922719(T;T)
Alt rs193922719(T;T)
Reference rs193922719(A;A)
Significance Probable-Pathogenic
Disease Hyperimmunoglobulin E syndrome
Variation info
Gene STAT3
CLNDBN Hyperimmunoglobulin E syndrome
Reversed 1
HGVS NC_000017.10:g.40475138T>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030468.1,