IL23R/C1orf141 rs78377598(PMID:26628628)
| Gene ID:149233/ 400757 |
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| Genotype:C/T |
| Functional Consequence:intron variant |
| Global MAF:T=0.0545/273 |
| DNA change: |
| Description: |
| Chromosome: |
| 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 |
|---|---|---|---|---|---|---|---|
| T | 18.8 | 5.3 | 4.1 | 1.02×10−3 | 2.04×10−3 |
| Function:Undone |
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