| Gene ID:337867 |
|---|
| Genotype:T/G |
| Functional Consequence:intron variant |
| Global MAF:T=0.4730/2369 |
| DNA change:c.928-5080G>T |
| Description:UBA domain containing 2 |
| Chromosome:13:99380148 |
| 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 |
|---|---|---|---|---|---|---|---|
| TT | |||||||
| TG | |||||||
| GG | |||||||
| T | |||||||
| G | 0.44 | 0.33 | 1.58 | 0.0071 |
| Function:Undone |
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