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. 2020 Feb 4;12:16. doi: 10.3389/fnagi.2020.00016

TABLE 3.

Association of SNPs of candidate genes and odds ratio to EOAD risk.

Gene SNP minor allele MAF (case/control) OR 95%CI P allele
HLA-DRB1 rs9271058 A 0.224/0.124 2.038 1.17–3.56 0.011
CD2AP rs9473117 C 0.102/0.134 0.733 0.36–1.50 0.393
PTK2B rs73223431 T 0.337/0.249 1.533 0.95–2.47 0.077

Gene SNP Dominant model (adjusted)
Recessive model (adjusted)
OR 95%CI P OR 95%CI P

HLA-DRB1 rs9271058 2.563 1.10–5.99 0.03 2.23 0.23–20.99 0.483
CD2AP rs9473117 0.327 0.12–0.93 0.035 0.69 0.08–5.88 0.231
PTK2B rs73223431 3.108 1.36–7.09 0.007 2.603 0.54–12.64 0.235

Gene SNP Additive model (adjusted)
Overdominant model (adjusted)
OR 95%CI P OR 95%CI P

HLA-DRB1 rs9271058 2.23 1.07–4.68 0.033 2.363 1.01–5.56 0.049
CD2AP rs9473117 0.39 0.16–0.93 0.034 0.387 0.13–1.16 0.09
PTK2B rs73223431 2.438 1.26–4.71 0.008 2.523 1.11–5.72 0.027

EOAD, early onset Alzheimer’s diseases; SNP, single nucleotide polymorphism; MAF, minor allele frequency; OR, odds ratio; CI, confidence interval. P allele was examined using the Chi-square test. P was adjusted for gender and age with binary logistic regression. Bold indicates statistically significant values.