FCGR3B rs1050501(PMID:19026120)

SNP information:
Gene ID:2215
Genotype:C/T
Functional Consequence:downstream variant 500B,missense
Global MAF:C=0.1859/931
DNA change:c.692T>C
Description:Fc fragment of IgG receptor IIIb
Chromosome:1:161674008
Article information:
Method:PCR
Population:Turkish Case:Control = 216:241
Related disease:Behcet's disease (BD) Year:2008
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
CC 32 0.148 50 0.208 0.108
CT 109 0.505 100 0.417
TT 75 0.347 90 0.375
C 139 0.322 190 0.399 1.13 0.016
T 293 0.678 286 0.601
Function:Undone
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