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Table 1 MAPT single SNPs association results with LOAD risk in the Mayo, ADGC and combined Mayo + ADGC cohorts

From: Association of MAPT haplotypes with Alzheimer’s disease risk and MAPT brain gene expression levels

SNP

A1

Mayo cohort

ADGC cohort

Mayo + ADGC

  

N

MAF_A

MAF_U

OR

95% CI

P

N

MAF_A

MAF_U

OR

95% CI

P

N

MAF_A

MAF_U

OR

95% CI

P

rs1467967

G

4,986

0.335

0.330

1.10

0.99 - 1.22

0.079

14,365

0.329

0.327

1.05

0.99 - 1.11

0.102

19,351

0.330

0.327

1.05

1.00 - 1.10

0.062

rs242557

A

4,935

0.377

0.379

1.00

0.90 - 1.11

0.988

13,407

0.358

0.356

1.01

0.95 - 1.07

0.721

18,342

0.363

0.364

1.00

0.95 - 1.05

0.974

rs3785883

A

5,247

0.182

0.183

1.07

0.95 - 1.22

0.274

15,187

0.178

0.171

1.08

1.01 - 1.15

0.032

20,434

0.179

0.175

1.06

1.01 - 1.13

0.034

rs2471738

T

5,282

0.223

0.209

1.07

0.95 - 1.21

0.250

14,181

0.207

0.201

1.05

0.98 - 1.12

0.194

19,463

0.209

0.203

1.05

0.99 - 1.11

0.109

rs8070723

G

5,129

0.209

0.222

0.81

0.71 - 0.91

7.0E-04

15,895

0.211

0.221

0.89

0.84 - 0.94

1.3E-04

21,024

0.211

0.221

0.90

0.85 - 0.95

5.3E-05

rs7521

A

5,171

0.458

0.457

1.08

0.97 - 1.19

0.152

15,656

0.466

0.468

1.02

0.97 - 1.07

0.529

20,827

0.465

0.465

1.02

0.97 - 1.06

0.437

  1. Results of multivariable logistic regression analyses are shown. CHR = chromosome. A1 = Minor Allele, N = number of subjects with genotype calls, A = Affected (LOAD subjects), U = Unaffected (Control), MAF = Minor Allele Frequency, OR = Odds Ratio, 95% CI = 95% Confidence intervals, P = p-value.
  2. Boldface values within the tables indicate significant or suggestive associations with a p-value <0.10.