FCRL3 rs11264799(PMID:19452015)

SNP information:
Gene ID:115352
Genotype:G/A
Functional Consequence:upstream variant 2KB,utr variant 5 prime
Global MAF:T=0.2712/1358
DNA change:c.-402G>A
Description:Fc receptor like 3 
Chromosome:1:157700967
Article information:
Method:PCR–RFLP
Population:Chinese Case:Control = 230:301
Related disease:Vogt–Koyanagi–Harada syndrome (VKH) Year:2009
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
AA 16 0.07 46 0.154 0.0127
AG 81 0.355 98 0.328 0.0127
GG 131 0.575 155 0.518 0.0127
A 113 0.248 190 0.318 0.707 0.0129
G 343 0.752 408 0.682 0.0129
Function:Undone
<<PREV NEXT>>