Table 2 Haplotype analysis for CFH, CFHR3 and CFHR5 single nucleotide polymorphisms (SNPs).
From: A haplotype in CFH family genes confers high risk of rare glomerular nephropathies
SNPs alleles | Haplotype frequency | Association test between rare kidney diseases and controls | ||||
|---|---|---|---|---|---|---|
rs55807605 | rs61737525 | rs57960694 | Cases (n = 91) | Controls (n = 300) | P-value* | OR (95% CI) |
G | C | G | 0.973 | 0.980 | 0.563 | 0.72 (0.25–2.08) |
A | C | G | 0.000 | 0.010 | 0.345 | 1.010 (1.002–1.018) |
A | T | A | 0.022 | 0.003 | 0.029 | 6.72 (1.22–36.99) |
G | T | G | 0.005 | 0.003 | 0.549 | 1.65 (0.15–18.32) |
A | C | A | 0.000 | 0.003 | 1.000 | 1.003 (0.999–1.008) |