TRIM39-RPP21 rs974963(PMID:20875797)

SNP information:
Gene ID:79897/202658
Genotype:G/T
Functional Consequence:missense,utr variant 3 prime
Global MAF:A=0.3726/1866
DNA change:c.1492C>A
Description:TRIM39-RPP21 readthrough
Chromosome:6:30346790
Article information:
Method:Genotyping Assay with BeadXpress
Population:Japanese Case:Control = 384:384
Related disease:Behcet's disease (BD) Year:2010
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
GG
GT
TT
G 0.665 0.541 1.73 6.4*10^-7
T
Function:Undone
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