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. 2022 Apr 2;7:112. doi: 10.1038/s41392-022-00923-1

Table 2.

Association results for selected SNPs in the discovery cohort and replication cohort and all cases and controls combined

SNP CHR BP (hg19) A1 F_A F_U A2 P-Discovery OR-Discovery F_A F_U P-Replication OR-Replication P-meta OR-Meta Gene Region
rs12995389 2 6485953 A 0.31 0.41 G 8.04 × 10−8 0.66 0.38 0.40 0.464 0.91 2.35 × 10−7 0.72 LOC400940;LINC01247 intergenic
rs9287675 2 6494761 A 0.24 0.32 G 5.03 × 10−7 0.66 0.30 0.31 0.817 0.97 3.37 × 10−6 0.73 LOC400940;LINC01247 intergenic
rs7598285 2 6505563 G 0.21 0.32 A 2.70 × 10−12 0.55 0.30 0.30 0.891 0.98 1.69 × 10−10 0.65 LINC01247 downstream
rs10519086 2 67262646 G 0.02 0.08 T 5.61 × 10−11 0.18 0.07 0.09 0.164 0.72 6.82 × 10−11 0.42 LINC01799;LINC01828 intergenic
rs72809129 2 77475663 A 0.24 0.35 C 6.97 × 10−10 0.59 0.43 0.47 0.268 0.87 1.42 × 10−9 0.67 LRRTM4 intronic
rs7422259 2 167377995 T 0.04 0.11 G 1.11 × 10−9 0.37 0.10 0.14 0.076 0.71 3.60 × 10−10 0.49 SCN7A;XIRP2 intergenic
rs4959041 6 30077967 C 0.25 0.27 T 6.90 × 10−6 0.92 0.23 0.25 0.279 0.86 5.88 × 10−6 0.91 TRIM31-AS1 ncRNA_intronic
rs9261445 6 30094788 T 0.23 0.26 G 4.37 × 10−7 0.86 0.23 0.25 0.298 0.86 5.30 × 10−7 0.86 TRIM31-AS1;TRIM40 intergenic
rs9261453 6 30099948 G 0.24 0.26 A 5.65 × 10−6 0.91 0.23 0.24 0.540 0.91 1.25 × 10−5 0.91 TRIM31-AS1;TRIM40 intergenic
rs9261484 6 30108683 T 0.26 0.29 C 7.14 × 10−6 0.89 0.24 0.26 0.492 0.91 1.33 × 10−5 0.89 TRIM40 intronic
rs9261496 6 30111014 T 0.25 0.26 C 7.88 × 10−6 0.91 0.22 0.25 0.410 0.89 1.11 × 10−5 0.91 TRIM40 intronic
rs9261502 6 30111610 T 0.24 0.26 A 4.51 × 10−6 0.91 0.22 0.24 0.568 0.92 1.11 × 10−5 0.91 TRIM40 intronic
rs9261521 6 30117773 T 0.22 0.25 C 2.61 × 10−8 0.81 0.24 0.25 0.860 0.97 3.17 × 10−7 0.85 TRIM40;TRIM10 intergenic
rs2069837 7 22768027 G 0.09 0.20 A 9.73 × 10−15 0.41 0.18 0.24 8.89 × 10−3 0.67 4.64 × 10−16 0.49 IL6 intronic
rs17158686 7 83794756 G 0.11 0.18 T 2.38 × 10−7 0.54 0.16 0.20 0.072 0.75 4.99 × 10−8 0.61 SEMA3A intronic

CHR chromosome, BP base-pair position (hg19), A1 Minor allele code, A2 major allele code, F_A frequency of this allele in cases, F_U frequency of this allele in controls, P logistic p value for association test, OR estimated odds ratio (for A1, i.e. A2 is reference), P-meta p value for METAL combined analysis