FGFR1OP rs2301436(PMID:23935994)

SNP information:
Gene ID:11116
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
Article information:
Method:PCR
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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