FCRL3 rs11264799(PMID:19050767)

SNP information:
Gene ID:115352
Genotype:C/T
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 = 245:289
Related disease:Behcet's disease (BD) Year:2008
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
AA 17 7.1 46 16 0.007 NS
AG 85 35.3 95 33
GG 139 57.7 147 51
A 119 24.7 187 32.5 0.7 0.0055 0.044
G 363 75.3 389 67.5 1.5
Allele/Genotype BD without HLA-B51 (N=146) Freq.Case Control without HLA-B51 (N=261) Freq.Control OR P value Pc value
AA 10 0.069 43 0.165 0.02 NS
AG 56 0.386 86 0.331
GG 79 0.545 131 0.504
A 76 0.26 172 0.331 0.7 0.04 NS
G 216 0.74 348 0.669 1.4
Function:Undone
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