| Gene ID:26191 |
|---|
| Genotype:G/C |
| Functional Consequence:intron variant,upstream variant 2KB |
| Global MAF:G=0.2530/1267 |
| DNA change:c.-1123C>G |
| Description:protein tyrosine phosphatase, non-receptor type 22 |
| Chromosome:1:113872746 |
| Method:PCR | |
|---|---|
| Population:Chinese | Case:Control = 1005:2010 |
| Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2014 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| GG | 102 | 0.101 | 310 | 0.154 | 0.62 | 7.06×10−5 | |
| CG | 454 | 0.452 | 1009 | 0.512 | 0.82 | 0.009 | |
| CC | 449 | 0.447 | 691 | 0.344 | 1.54 | 3.86×10−8 | |
| G | 658 | 0.327 | 1629 | 0.405 | 0.71 | 4.25×10−9 | |
| C | 1352 | 0.673 | 2391 | 0.595 | 1.4 | 4.25×10−9 |
| Function:Done |
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