| Gene ID:84959 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant,upstream variant 2KB |
| Global MAF:T=0.3894/1950 |
| DNA change:c.162-5841T>C |
| Description:ubiquitin associated and SH3 domain containing B |
| Chromosome:11:122770378 |
| Method:TaqMan SNP Genotyping Assays | |
|---|---|
| Population:Turk | Case:Control = 152:172 |
| Related disease:Behcet's disease (BD) | Year:2009 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| T | 161 | 56.7 | 125 | 43.4 | 1.71 | 1.5 × 10-3 | 0.0195 |
| Function:Undone |
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