| Gene ID:414778/3139 |
|---|
| Genotype:A/G |
| Functional Consequence:intron variant,nc transcript variant |
| Global MAF:T=0.3976/1991 |
| DNA change: |
| Description:HLA complex group 17 |
| Chromosome:6:30261680 |
| Method:Genotyping Assay with BeadXpress | |
|---|---|
| Population:Japanese | Case:Control = 384:384 |
| Related disease:Behcet's disease (BD) | Year:2010 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| TT | |||||||
| TC | |||||||
| CC | |||||||
| T | |||||||
| C | 0.66 | 0.545 | 1.66 | 4.1*10^-6 |
| Function:Undone |
|---|
| <<PREV | NEXT>> |
|---|