IL23R rs117633859(PMID:25108386)
| Gene ID:149233 |
|---|
| Genotype:A/G |
| Functional Consequence:intron variant |
| Global MAF:G=0.0407/204 |
| DNA change: |
| Description: |
| Chromosome: |
| Method:Beadchip and GeneChip | |
|---|---|
| Population:Chinese | Case:Control = 1599:5640 |
| Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2014 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| A | |||||||
| G | 16 | 9.5 | 1.82 | 3.42 × 10−21 |
| Function:Done |
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