IL23R/C1orf141 rs12561798(PMID:26628628)
Gene ID:149233/400757 |
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Genotype:C/T |
Functional Consequence:intron variant,upstream variant 2KB |
Global MAF:C=0.0511/256 |
DNA change:c.-1655A>G |
Description:interleukin 23 receptor-chromosome 1 open reading frame 141 |
Chromosome:1:67136481 |
Method:Sequenom MassARRAY system;Taqman SNP assays | |
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Population:Chinese Singaporean | Case:Control = 32:94 |
Related disease:Vogt–Koyanagi–Harada syndrome (VKH) | Year:2016 |
Allele/Genotype | Case | Freq.Case | Control | Freq.Control | OR(95%CI) | P value | Pc value |
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C | 18.8 | 3.7 | 5.9 | 8.49×10−5 | 1.69×10−4 |
Function:Undone |
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