Skip to main content
. 2022 Jun 6;7(3):336–344. doi: 10.1089/can.2021.0046

Table 2.

Summary of Genomic Testing Results of Cannabinoid Hyperemesis Syndrome Patients Versus Controls

Gene RSID Mutation Allele Zygosity Diplotype Haplotype p a Odds ratio (confidence interval) Control displaying variant (%) CHS patients displaying variant
COMT rs4646316 Intron C>T Heterozygous CGGC/TGGC CGGC 0.012 12 (1.3–98.1) 10 57.1%
ABCA1 rs2230806 Synonymous C>T Homozygous CTTG/CTTG CTTG 0.012 8.4 (1.5–48.1) 20 67.9%
TRPV1 rs879207 Downstream A>G Heterozygous ATGG/GTGG ATGG 0.015 5.8 (1.2–28.4) 30 71.5%
DRD2 rs4648318 Intron T>C Heterozygous TCCC/CCCC TCCC 0.031 6.2 (1.1–34.7) 20 60.7%
CYP2C9 rs1934967 Intron C>T Homozygous CTTG/CTTG CTTG 0.043 (0.011b) 7.8 (1.1–70.1) 10 46.4% (60%b)
TRPV1 rs11655540 Intron T>G Heterozygous TCAA/GCAA TCAA 0.066 4.2 (0.8–19.9) 30 64.3%
COMT rs165656 Intron C>T Heterozygous CCGG/TCGG CCGG 0.069 4.6 (0.8–25.7) 20 53.6%
CYP2C19 rs4494250 Intron G>A Heterozygous GCTT/ACTT GCTT 0.069 (0.007b) 4.6 (0.8–25.7) 20 53.6% (75%b)
CRY1 rs2287161 Downstream G>C Heterozygous GTCG/CTCG GTCG 0.091 3.7 (0.8–16.9) 50 78.6%
a

p-Values were obtained through a Fisher exact test. Odds ratios are shown with a 95% confidence interval.

b

Genes CYP2C9 and CYP2C19 have a second set of values showing when patients on PPI medications were excluded from the data. This was due to suspected interactions of CYP2C9 and CYP2C19 and PPI medication.