| Gene ID:149233/3595 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant |
| Global MAF:A=0.3379/1692 |
| DNA change:c.1149-2391G>A |
| Description:interleukin 23 receptor-interleukin 12 receptor subunit beta 2 |
| Chromosome:1:67253446 |
| Method:Sequenom iPlex assay | |
|---|---|
| Population:Iranian | Case:Control = 973:637 |
| Related disease:Behcet's disease (BD) | Year:2012 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| T | 0.72 | 0.0002 | 0.000187 |
| Function:undone |
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