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.
