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Table 4 Phenotype-genotype correlation

From: The common NOD2/CARD15 variant P268S in patients with non-infectious uveitis: a cohort study

  No mutation He Ho p-value
P268/SNP5 P268/SNP5
Comorbility, % (n) 5 9 50 % (1) n.s.
Positive family history, % (n) 1 4 50 % (1) n.s.
Granulomatous uveitis, % (n) 0 5 0 n.s.
Panuveitis, % (n) 3 9 0 n.s.
Bilateral uveitis, % (n) 6 8 50 % (1) n.s.
ANA positive, % (n) 3 7 50 % (1) n.s.
HLA B27 positive, % (n) 0 2 0 n.s.
Macular edema, % (n) 3 7 0 n.s.
Synechiae, % (n) 2 4 1 n.s.
Glaucoma, % (n) 2 2 0 n.s.
Visual loss, % (n) 2 3 0 n.s.
Cataract, % (n) 2 1 0 n.s.
He = heterozygous; Ho = homozygous     n.s.