rs4143832
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4143832(A;A) |
| Make rs4143832(A;C) |
| Make rs4143832(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 132527285 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4143832 |
| dbSNP (classic) | rs4143832 |
| ClinGen | rs4143832 |
| ebi | rs4143832 |
| HLI | rs4143832 |
| Exac | rs4143832 |
| Gnomad | rs4143832 |
| Varsome | rs4143832 |
| LitVar | rs4143832 |
| Map | rs4143832 |
| PheGenI | rs4143832 |
| Biobank | rs4143832 |
| 1000 genomes | rs4143832 |
| hgdp | rs4143832 |
| ensembl | rs4143832 |
| geneview | rs4143832 |
| scholar | rs4143832 |
| rs4143832 | |
| pharmgkb | rs4143832 |
| gwascentral | rs4143832 |
| openSNP | rs4143832 |
| 23andMe | rs4143832 |
| SNPshot | rs4143832 |
| SNPdbe | rs4143832 |
| MSV3d | rs4143832 |
| GWAS Ctlg | rs4143832 |
| GMAF | 0.2002 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19198610] |
| Trait | Plasma eosinophil count |
| Title | Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction |
| Risk Allele | C |
| P-val | 1E-10 |
| Odds Ratio | 7.10 [4.9-9.2] % standard unit increase |
[PMID 18056382
] Analysis of the 5q31 33 locus shows an association between single nucleotide polymorphism variants in the IL-5 gene and symptomatic infection with the human blood fluke, Schistosoma japonicum.
[PMID 18614543] The 5q31 variants associated with psoriasis and Crohn's disease are distinct.
[PMID 19860791] Genetic evidence for a role of IL33 in nasal polyposis.
[PMID 23328882] Meta-analyses of four eosinophil related gene variants in coronary heart disease.
