TLR8 rs2407992(PMID:26486764)

SNP information:
Gene ID:51311
Genotype:C/G
Functional Consequence:intron variant,synonymous codon
Global MAF:G=0.2771/1046
DNA change:c.2007G>A
Description:toll like receptor 8
Chromosome:X:12920993
Article information:
Method:SEQUENOM iPlex MassARRAYplatform
Population:Spanish Case:Control = 371:1385
Related disease:Behcet's disease (BD) Year:2015
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
CC
CG
GG
C 170 0.458 367 0.386 1.34 0.0025 0.0141
G
Allele/Genotype Female BD (N=211) Freq.Case Female Control (N=824) Freq.Control OR P value Pc value
CC
CG
GG
C 0.445 0.38 1.31 0.012
G
Allele/Genotype Male BD (N=160) Freq.Case Male Control (N=561) Freq.Control OR P value Pc value
CC
CG
GG
C 0.473 0.403 1.33 0.11
G
Function:Undone
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