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Table 3 SNP associated with the development of nonalcoholic fatty liver disease

From: The association of genetic polymorphisms with nonalcoholic fatty liver disease in a longitudinal study

  Discovery Validation
SNP Chr Position Nearest Genes Risk
Risk allele Frequency HR
(95% CI)
P-value Risk allele Frequency HR
(95% CI)
rs4906353 14 104,127,246 KCL1 T 0.030 0.72
(0.61, 0.85)
9.68E-5 0.026 0.65
(0.48, 0.88)
  1. SNP single-nucleotide polymorphism, Chr chromosome number, HR hazard ratio, CI confidence interval, KCL kinesin light chain
  2. P values are adjusted for age, sex and body mass index. An additive genetic model was used