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. Author manuscript; available in PMC: 2020 Nov 5.
Published in final edited form as: Subst Use Misuse. 2019 Jan 20;54(4):670–680. doi: 10.1080/10826084.2018.1531430

Table 2.

Association of SNPs and VNTRs with cannabis use. Genotype and allele frequency analyses.

SNP ID (gene) Genotypes and Alleles Subjects Fisher’s exact test SNP ID / VNTR (gene) Genotypes and Alleles Subjects Fisher’s exact test
CTRLs MJ users CTRLs MJ users
rs1049353 (CNR1) GG 61.8% 52.17% 0.051(*) rs6277 (DRD2) CC 11.83% 16% 0.51
AA 4.30% 0.00% TT 29.03% 33%
GA 38.20% 47.83% CT 59.14% 51%
G allele 80.90% 76.09% 0.3 C allele 41.40% 41.85% 1
A allele 19.10% 23.91% T allele 58.60% 58.15%

rs324420 (FAAH)
CC 62.37% 68.48% 0.52
rs1800497 (ANKK1)
CC 76.34% 57.61% 0.034
AA 6.45% 3.26% TT 2.15% 4.35%
CA 31.18% 28.26% TC 21.51% 38.04%
C allele 77.96% 82.61% 0.29 C allele 87.10% 76.63% 0.032
A allele 22.04% 17.39% T allele 12.90% 23.37%

rs4680 (COMT)
GG 33.33% 31.52% 0.97
VNTR 3’UTR (DAT1)
9R/9R 10.75% 7.61% 0.81
AA 16.13% 16.30% 10R/10R 43.01% 44.57%
GA 50.54% 52.17% 9R/10R 43.01% 43.48%
G allele 58.60% 57.61% 0.91 9R 65.57% 67.78% 0.73
A allele 41.40% 42.39% 10R 34.43% 32.22%
VNTR-48 bp (DRD4) R<7 (S) 84.41% 88.04% 0.36 (**)
R≥7 (L) 15.59% 11.96%
(*)

Due to the lack of a reasonable number of homozygous A/A subjects, for the SNP rs1049353, Fisher’s exact test was performed in two different ways, including and excluding A/A homozygous subjects (no significant differences were revealed excluding A/A subjects).

(**)

For DRD4 VNTR, since the high number of alleles, the number of observations does not allow the statistical analysis for the genotype distribution; in this case statistical analysis is reported only on alleles.