| Gene ID:337867 |
|---|
| Genotype:A/C/G |
| Functional Consequence:intron variant |
| Global MAF:A=0.4331/2169 |
| DNA change:c.390-33429G>A |
| Description:UBA domain containing 2 |
| Chromosome:13:99280668 |
| 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 |
|---|---|---|---|---|---|---|---|
| G | 0.48 | 0.34 | 1.78 | 0.00058 |
| Function:done |
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