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. 2019 Oct 29;57(2):1035–1043. doi: 10.1007/s12035-019-01798-0

Table 1.

Results of the association analysis using recessive (a) single- and (b) multi-locus linear mixed-effect models for ADAOO in 71 patients with PSEN1 E280A Alzheimer’s disease

(a)
Chr SNPa Position Gene Marker Information Single-locus linear mixed-effects model
Ref/Alt MAF CR Change β^SEβ^ P PFDR
3 rs9809384 111,981,878 SL9C1 T/C 0.32 1 p.Ile364Val 9.73 (1.61) 8.06 × 10−8 1.8 × 10−3
3 rs9809404 111,981,924 SL9C1 T/C 0.29 1 p.Ile348Met 10.85 (1.80) 8.13 × 10−8 9.2 × 10−4
(b)
Chr SNPa Position Gene Marker Information Multi-locus linear mixed-effects model
Ref/Alt MAF CR Change β^SEβ^ P PFDR
3 rs9809384 111,981,878 SLC9C1 T/C 0.32 1 p.Ile364Val 11.03 (1.06) 1.77 × 10−15 4.05 × 10−11
4 rs10030475 70,807,771 CSN1S1 C/T 0.42 0.97 p.Ala117Val 6.37 (0.94) 4.76 × 10−9 5.43 × 10−5
10 rs33995374 100,020,880 LOXL4 C/T 0.2 0.98 p.Arg154Gln 8.80 (1.55) 3.28 × 10−7 2.4 × 10−3
14 rs2273946 24,458,162 DHRS4L2 G/C 0.32 0.98 p.Gln2His -8.13 (1.43) 3.48 × 10−7 1.9 × 10−3

aUCSC GRCh37/hg19 coordinates. AOO, age of onset; Chr, chromosome; SNP, single-nucleotide polymorphism; Ref/Alt, reference/alternate allele; MAF, minimum allele frequency; CR, call rate; β^, regression coefficient; SEβ^, standard error of β^; P , P value; FDR, false discovery rate. Highlighted variants accelerate ADAOO