| Gene ID:3627 |
|---|
| Genotype:C/T |
| Functional Consequence:intron variant,utr variant 3 prime |
| Global MAF:T=0.1855/929 |
| DNA change:c.*519G>A |
| Description:C-X-C motif chemokine ligand 12 |
| Chromosome:10:44372809 |
| Method:Real-Time PCR | |
|---|---|
| Population:Chinese Han | Case:Control = 368:547 |
| Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2017 |
| Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
|---|---|---|---|---|---|---|---|
| CC | 223 | 0.605 | 271 | 0.495 | 1.566 | 0.001 | |
| CT | 122 | 0.331 | 241 | 0.441 | 0.637 | 9.443×10−4 | |
| TT | 23 | 0.062 | 35 | 0.064 | 0.975 | 0.928 | |
| C | 568 | 0.771 | 783 | 0.716 | 1.343 | 0.008 | |
| T | 168 | 0.228 | 311 | 0.284 | 0.745 |
| Function: |
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