| Gene ID:26191 |
|---|
| Genotype:A/G |
| Functional Consequence:intron variant,missense |
| Global MAF:A=0.0274/137 |
| DNA change: |
| Description: |
| Chromosome: |
| Method:SSP–PCR | |
|---|---|
| Population:United Kingdom and Middle East | Case:Control = 270:234 |
| Related disease:Behcet's disease (BD) | Year:2007 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| CC | |||||||
| CT | |||||||
| TT | |||||||
| C | 525 | 15 | 0.028 | ||||
| T | 438 | 30 | 0.068 | 2.4 | 0.005 |
| Function:Udone |
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