Gene ID:11116 |
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Genotype:A/G |
Functional Consequence:intron variant |
Global MAF:T=0.3682/1844 |
DNA change:c.666-282C>T |
Description:C-C motif chemokine receptor 6 |
Chromosome:6:167024500 |
Method:PCR | |
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Population:Chinese Han | Case:Control = 601:725 |
Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2013 |
Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
---|---|---|---|---|---|---|---|
GG | 110 | 0.183 | 1749 | 0.247 | 0.068 | ||
AA | 195 | 0.323 | 201 | 0.277 | 0.136 | ||
AG | 297 | 0.494 | 345 | 0.476 | 0.903 | ||
A | 685 | 0.57 | 747 | 0.515 | 0.044 | ||
G | 517 | 0.43 | 703 | 0.485 | 0.044 |
Function:Undone |
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