rs5744241
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs5744241(A;G) |
| Make rs5744241(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 112156421 |
| Gene | IL18 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5744241 |
| dbSNP (classic) | rs5744241 |
| ClinGen | rs5744241 |
| ebi | rs5744241 |
| HLI | rs5744241 |
| Exac | rs5744241 |
| Gnomad | rs5744241 |
| Varsome | rs5744241 |
| LitVar | rs5744241 |
| Map | rs5744241 |
| PheGenI | rs5744241 |
| Biobank | rs5744241 |
| 1000 genomes | rs5744241 |
| hgdp | rs5744241 |
| ensembl | rs5744241 |
| geneview | rs5744241 |
| scholar | rs5744241 |
| rs5744241 | |
| pharmgkb | rs5744241 |
| gwascentral | rs5744241 |
| openSNP | rs5744241 |
| 23andMe | rs5744241 |
| SNPshot | rs5744241 |
| SNPdbe | rs5744241 |
| MSV3d | rs5744241 |
| GWAS Ctlg | rs5744241 |
| GMAF | 0.03994 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22015107] Interleukin 18 gene variation and risk of acute myocardial infarction
[PMID 20478055
] Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study.
