| Gene ID:149233/400757 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant,upstream variant 2KB |
| Global MAF:G=0.1504/753 |
| DNA change:c.-103-209C>T |
| Description:interleukin 23 receptor-chromosome 1 open reading frame 141 |
| Chromosome:1:67131436 |
| Method:Sequenom MassARRAY system;Taqman SNP assays | |
|---|---|
| Population:Chinese Singaporean | Case:Control = 32:94 |
| Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2016 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| C | 20.3 | 4.8 | 5 | 1.46×10−4 | 2.92×10−4 |
| Function:Undone |
|---|
| <<PREV | NEXT>> |
|---|