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rs2269426

From SNPedia

Orientationminus
Stabilizedminus
Make rs2269426(C;C)
Make rs2269426(C;T)
Make rs2269426(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32108722
GeneTNXB
is asnp
is mentioned by
dbSNPrs2269426
ebirs2269426
HLIrs2269426
Exacrs2269426
Varsomers2269426
Maprs2269426
PheGenIrs2269426
hapmaprs2269426
1000 genomesrs2269426
hgdprs2269426
ensemblrs2269426
gopubmedrs2269426
geneviewrs2269426
scholarrs2269426
googlers2269426
pharmgkbrs2269426
gwascentralrs2269426
openSNPrs2269426
23andMers2269426
23andMe allrs2269426
SNP Nexus

SNPshotrs2269426
SNPdbers2269426
MSV3drs2269426
GWAS Ctlgrs2269426
GMAF0.3393
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19198610]
Trait Plasma eosinophil count
Title Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Risk Allele T
P-val 0.000003
Odds Ratio 4.60 [2.7-6.6] % standard unit increase



[PMID 19860791] Genetic evidence for a role of IL33 in nasal polyposis.


[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


GET Evidence
rs2269426
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.309524
summary