| Gene ID:51752 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant,missense |
| Global MAF:T=0.4038/2022 |
| DNA change: |
| Description: |
| Chromosome: |
| Method:Illumina immunochip infinium microarray | |
|---|---|
| Population:European | Case:Control = 1422:2339 |
| Related disease:Acute anterior uveitis (AAU) | Year:2014 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| T | 0.873 | 0.0177 | NS | ||||
| C | |||||||
| Anklosing spomdylitis (AS) with AAU | Anklosing spomdylitis (AS) without AAU |
| Function:Undone |
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