rs2058660
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2058660(C;C) |
| Make rs2058660(C;T) |
| Make rs2058660(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 2 |
| Position | 102437989 |
| Gene | IL18RAP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2058660 |
| dbSNP (classic) | rs2058660 |
| ClinGen | rs2058660 |
| ebi | rs2058660 |
| HLI | rs2058660 |
| Exac | rs2058660 |
| Gnomad | rs2058660 |
| Varsome | rs2058660 |
| LitVar | rs2058660 |
| Map | rs2058660 |
| PheGenI | rs2058660 |
| Biobank | rs2058660 |
| 1000 genomes | rs2058660 |
| hgdp | rs2058660 |
| ensembl | rs2058660 |
| geneview | rs2058660 |
| scholar | rs2058660 |
| rs2058660 | |
| pharmgkb | rs2058660 |
| gwascentral | rs2058660 |
| openSNP | rs2058660 |
| 23andMe | rs2058660 |
| SNPshot | rs2058660 |
| SNPdbe | rs2058660 |
| MSV3d | rs2058660 |
| GWAS Ctlg | rs2058660 |
| GMAF | 0.2778 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21102463 ]
|
| Trait | |
| Title | Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci |
| Risk Allele | G |
| P-val | 2E-12 |
| Odds Ratio | 1.1900 [1.14-1.26] |
[PMID 23103228] Identification of IL18RAP/IL18R1 and IL12B as leprosy risk genes demonstrates shared pathogenesis between inflammation and infectious diseases.
