rs2269426
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2269426(C;C) |
Make rs2269426(C;T) |
Make rs2269426(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32108722 |
Gene | TNXB |
is a | snp |
is | mentioned by |
dbSNP | rs2269426 |
dbSNP (classic) | rs2269426 |
ClinGen | rs2269426 |
ebi | rs2269426 |
HLI | rs2269426 |
Exac | rs2269426 |
Gnomad | rs2269426 |
Varsome | rs2269426 |
LitVar | rs2269426 |
Map | rs2269426 |
PheGenI | rs2269426 |
Biobank | rs2269426 |
1000 genomes | rs2269426 |
hgdp | rs2269426 |
ensembl | rs2269426 |
geneview | rs2269426 |
scholar | rs2269426 |
rs2269426 | |
pharmgkb | rs2269426 |
gwascentral | rs2269426 |
openSNP | rs2269426 |
23andMe | rs2269426 |
SNPshot | rs2269426 |
SNPdbe | rs2269426 |
MSV3d | rs2269426 |
GWAS Ctlg | rs2269426 |
GMAF | 0.3393 |
Max Magnitude | 0 |
? | (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 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.