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. 2022 Sep 5;3(4):1042–1052. doi: 10.1016/j.bpsgos.2022.08.006

Table 1.

Significant SNPs Identified From Genome-wide Analysis of REYD in Discovery and Replication Samples and Meta-analyses


CHR
SNP Pos A1 LD With rs75885813 β
SE
Coefficient t-Statistic
p
Discovery Replication Discovery Replication Discovery Replication Discovery Replication Meta-analysis
16 rs75885813 7,141,263 T −0.669 −0.276 0.112 0.130 −5.96 −2.12 3.83 × 10−9 0.034 3.67 × 10−9
16 rs114891671 7,142,203 C 0.98 −0.669 −0.352 0.113 0.135 −5.90 −2.60 5.56 × 10−9 0.0094 6.04 × 10−10
16 rs115712598 7,142,236 T 0.98 −0.669 −0.352 0.113 0.135 −5.90 −2.60 5.56 × 10−9 0.0094 6.04 × 10−10
16 rs116183707 7,142,287 A 0.98 −0.669 −0.352 0.113 0.135 −5.90 −2.60 5.56 × 10−9 0.0094 6.04 × 10−10
16 rs7205995 7,140,331 G 0.98 −0.667 −0.35 0.113 0.135 −5.88 −2.59 6.05 × 10−9 0.0097 6.69 × 10−10

Five whole-genome–significant SNPs that are in high LD were identified (r2 > 0.8).

CHR, chromosome; LD, linkage disequilibrium; Pos, position; REYD, Rey Complex Figure Test Delayed Component; SNP, single nucleotide polymorphism.