| Gene ID:337867 |
|---|
| Genotype:C/G |
| Functional Consequence:intron variant |
| Global MAF:C=0.4543/2275 |
| DNA change:c.32-18248G>A |
| Description:UBA domain containing 2 |
| Chromosome:13:99220179 |
| Method:TaqMan SNP Genotyping Assays | |
|---|---|
| Population:Turk | Case:Control = 676:1096 |
| Related disease:Behcet's disease (BD) | Year:2011 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| CC | |||||||
| CG | |||||||
| GG | |||||||
| C | |||||||
| G | 0.46 | 0.34 | 1.65 | 0.0043 |
| Function:Undone |
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