TABLE 4.
All Caucasian Datasets Excluding Toronto Dataset
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All Caucasian Datasets
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SNP | Allele1 | Allele2 | Weight | Zscore | p | Direction | I2 | p(Q)a | Allele1 | Allele2 | Weight | Zscore | p | Directiona | I2 | p(Q) |
1 | Not genotyped in NIA-LOAD | Not genotyped in NIA-LOAD | ||||||||||||||
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2 | c | g | 3967 | 0.881 | 0.37 | +++ | 0.22 | 0.92 | c | g | 4639 | 1.018 | 0.3 | ++++ | 0.23 | 0.92 |
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3 | Not polymorphic | Not polymorphic | ||||||||||||||
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4 | a | g | 3967 | −2.769 | 0.005 | − − − | 0.34 | 0.9 | a | g | 4639 | −1.75 | 0.08 | − − −+ | 4.21 | 0.9 |
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5 | t | c | 3967 | 2.693 | 0.007 | +++ | 0.12 | 0.9 | t | c | 4639 | 1.618 | 0.1 | +++− | 3.12 | 0.9 |
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6 | Not genotyped in MIRAGE Caucasian | Not genotyped in MIRAGE | ||||||||||||||
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7 | a | g | 3967 | −3.153 | 0.001 | − − − | 0.32 | 0.9 | a | g | 4639 | −2.182 | 0.03 | − − −+ | 6.14 | 0.9 |
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8 | t | c | 3967 | −3.334 | 0.0008 | − − − | 0.24 | 0.9 | t | c | 4639 | −2.405 | 0.01 | − − −+ | 5.27 | 0.9 |
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9 | t | c | 3967 | −2.895 | 0.003 | − − − | 5.23 | 0.7 | t | c | 4639 | −1.909 | 0.05 | − − −+ | 6.48 | 0.7 |
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10 | t | g | 3967 | −0.319 | 0.74 | +− − | 9.47 | 0.4 | t | g | 4639 | −0.359 | 0.71 | +333 | 8.84 | 0.4 |
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11 | a | g | 3967 | 1.892 | 0.06 | +++ | 7.86 | 0.5 | a | g | 4639 | 1.348 | 0.17 | +++− | 7.96 | 0.5 |
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12 | a | g | 3967 | 0.15 | 0.88 | −+ − | 16.13 | 0.3 | a | g | 4639 | −0.06 | 0.95 | −+ − − | 15.42 | 0.3 |
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13 | t | c | 3967 | 2.168 | 0.03 | +++ | 14.1 | 0.3 | t | c | 4639 | 1.784 | 0.07 | +++− | 14.14 | 0.3 |
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14 | t | c | 3967 | 0.902 | 0.36 | +− − | 18.26 | 0.3 | t | c | 4639 | 1.047 | 0.29 | +− −+ | 16.93 | 0.3 |
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15 | c | g | 3967 | 0.999 | 0.31 | ++− | 0.43 | 0.9 | c | g | 4639 | 0.806 | 0.42 | ++− | 2.31 | 0.9 |
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16 | Not genotyped in MIRAGE Caucasian/Miami | Not genotyped in MIRAGE Caucasian/Miami |
All p values of ≤0.05 are in bold. All p values that are close to statistical significance (0.05 ≤p ≤ 0.1) are in italics. SNPs that are associated with a changed risk for AD in at least 2 independent data sets are underlined.
Heterogeneity (Cochran’s Q) p-value.
χ2 = chi square test statistic; AD = Alzheimer’s disease; SNP = single-nucleotide polymorphism.