| Gene ID:7128 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant,nc transcript variant |
| Global MAF:C=0.2061/1032 |
| DNA change: |
| Description:TNF alpha induced protein 3 |
| Chromosome:6:137851611 |
| Method:PCR | |
|---|---|
| Population:Chinese Han | Case:Control = 834:1415 |
| Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2013 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| CC | 9 | 0.011 | 10 | 0.007 | 1.5 | NS | |
| CT | 228 | 0.273 | 264 | 0.187 | 1.6 | 2.26*10^-5 | |
| TT | 597 | 0.716 | 1141 | 0.806 | 0.6 | 1.12*10^-5 | |
| C | 246 | 0.147 | 284 | 0.1 | 1.6 | 1.09*10^-5 | |
| T |
| Function:Undone |
|---|
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