Table 3.
NO. | SNP1×SNP2 | GENE | CHR | Main Effect | Interaction | Explained Variance (R Square) | |||||
---|---|---|---|---|---|---|---|---|---|---|---|
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p-value | p-value | Corrected p-value | Age+Gendera | Dxb | APOEc | SNP1+SNP2d | SNP1* SNP2e | ||||
1 | rs1514061× | PLXNA4* | 7 | 3.41E-06 | 8.35E-10 | 0.0181 | 0.01 | 0.164 | 0.129 | 0.015 | 0.051 |
rs6467419 | PLXNA4* | 7 | 0.00167353 | ||||||||
| |||||||||||
2 | rs1514061× | PLXNA4* | 7 | 3.41E-06 | 1.97E-10 | 0.0043 | 0.01 | 0.164 | 0.129 | 0.019 | 0.047 |
rs4453471 | CDH13 | 16 | 0.00377003 | ||||||||
| |||||||||||
3 | rs7303599× | ADIPOR2* | 12 | 7.91E-05 | 5.76E-11 | 0.0013 | 0.01 | 0.164 | 0.129 | 0.023 | 0.042 |
rs7146454 | ADSSL1* | 14 | 0.00733134 | ||||||||
| |||||||||||
4 | rs7303599× | ADIPOR2* | 12 | 7.91E-05 | 6.91E-10 | 0.0150 | 0.01 | 0.164 | 0.129 | 0.021 | 0.041 |
rs167396 | GSN* | 9 | 0.00583631 | ||||||||
| |||||||||||
5 | rs1482548× | INHBA* | 7 | 0.007007 | 2.95E-10 | 0.0064 | 0.01 | 0.164 | 0.129 | 0.015 | 0.038 |
rs12894119 | NIN* | 14 | 0.00867969 | ||||||||
| |||||||||||
6 | rs9550406× | MTUS2* | 13 | 0.00543688 | 1.49E-09 | 0.0324 | 0.01 | 0.164 | 0.129 | 0.010 | 0.034 |
rs6471951 | RLBP1L1 | 8 | 0.00604041 | ||||||||
| |||||||||||
7 | rs211953× | CXADR | 21 | 0.000478713 | 3.03E-10 | 0.0066 | 0.01 | 0.164 | 0.129 | 0.024 | 0.031 |
rs4881147 | PITRM1* | 10 | 0.0015086 |
The Bonferroni corrected p-values (< 0.05) and R2 of the SNP*SNP interaction term are shown in bold.
Age+Gender: Percent of variance in T-tau/Aβ42 level explained by age, gender.
Dx: Percent of variance in T-tau/Aβ42 level explained by diagnosis after accounting for age, gender.
APOE: Percent of additional variance in T-tau/Aβ42 level explained by the APOE genotype after accounting for age, gender and diagnosis.
SNP1+SNP2: Percent of additional variance in T-tau/Aβ42 level explained by the combined main effect of SNP1 and SNP2 after accounting for age, gender, diagnosis, and the APOE genotype.
SNP1*SNP2: Percent of additional variance in T-tau/Aβ42 level explained by the interaction effect of SNP1 and SNP2 after accounting for age, gender, diagnosis, APOE genotype, SNP1 and SNP2.
Nearest gene proximal to the SNP.