Table 1.
SNP rs | Chr | Gene | BP | A1 | A2 | Freq A1 | N | β | SE | p-value | Direction |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2875907 | 3p12.1 | CADM2 | 85,518,580 | A | G | 0.352 | 181,675 | 0.070 | 0.009 | 9.38e-17 | +++ |
rs1448602 | 3p12.1 | CADM2 | 85,780,454 | A | G | 0.756 | 184,765 | -0.062 | 0.010 | 6.55e-11 | --- |
rs7651996 | 3p12.1 | CADM2 | 85,057,349 | T | G | 0.477 | 184,765 | 0.049 | 0.008 | 2.37e-09 | +++ |
rs10085617 | 7p22.2 | SDK1 | 3,634,711 | A | T | 0.416 | 184,765 | 0.046 | 0.008 | 2.93e-08 | +++ |
rs9773390 | 8q21.13 | ZNF704 | 81,565,692 | T | C | 0.933 | 44,595 | -0.171 | 0.029 | 5.66e-09 | --? |
rs9919557 | 11q23.2 | NCAM1 | 112,877,408 | T | C | 0.614 | 180,428 | -0.055 | 0.009 | 9.94e-11 | --- |
rs10499 | 16p11.2 | RABEP2, ATP2A1 | 28,915,527 | A | G | 0.651 | 179,767 | 0.053 | 0.009 | 1.13e-09 | +++ |
rs17761723 | 17p13.3 | SMG6 | 2,107,090 | T | C | 0.346 | 184,765 | 0.047 | 0.009 | 3.24e-08 | +++ |
Independent hits were defined as R2<0.01, window size 250 kb. The p-value threshold was set at p<5e-08 (conventional genome-wide significant threshold; significance was tested two-sided). Chromosomal region (Chr), gene the SNP is located in or the nearest gene (within 500kb; Gene), base pairs location SNP on Hg19 (BP), allele 1 (A1), allele 2 (A2), frequency of allele 1 (Freq A1), number of individuals for which variant was included (N), beta coefficient of the effect allele A1 (β), standard error (SE).
Direction per sample: allele A1 increases (+) or decreases (−) liability for cannabis use, or sample did not contribute to this SNP (?). Order of samples: ICC, 23andMe, UK-Biobank. Independent SNPs were selected as SNPs with linkage disequilibrium R2<0.1 using a window size of 250 kB.