CFH rs1061170(PMID:19001225)

SNP information:
Gene ID:3075
Genotype:C/T
Functional Consequence:missense,nc transcript variant
Global MAF:C=0.2666/1335
DNA change:c.1204C
Description:complement factor H
Chromosome:1:196690107
Article information:
Method:PCR
Population:American Case:Control = 96:736
Related disease:Multifocal choroiditis (MFC) Year:2008
Allele/Genotype Case Freq.Case Control Freq.Control OR(95%CI) P value Pc value
C 0.553 0.324 2.46 <0.001
T
Function:Undone
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