Table 2. Variants in the CaMKIV gene are associated with nicotine dependence.
Phenotype | SNP | Allele | P-value | Beta/OR | Q p-value |
FTND | rs919334 | C | 0.01 | −0.185 | 0.41 |
rs1457115 | A | 0.53 | −0.044 | 0.51 | |
rs9285875 | T | 0.04 | 0.163 | 0.82 | |
numCIG | rs919334 | C | 0.17 | −0.034 | 0.20 |
rs1457115 | A | 0.95 | −0.001 | 0.45 | |
rs9285875 | T | 0.43 | 0.021 | 0.88 | |
FTND1 | rs919334 | C | 0.14 | −0.045 | 0.06 |
rs1457115 | A | 0.11 | 0.046 | 0.86 | |
rs9285875 | T | 0.63 | −0.015 | 0.56 | |
FTND5 | rs919334 | C | 0.33 | 0.94 | 0.02 |
rs1457115 | A | 0.50 | 1.04 | 0.72 | |
rs9285875 | T | 0.87 | 1.01 | 0.08 |
Human genetic association meta-analysis using two datasets (SAGE and MGS, n = 3,969). The variant rs919334 is associated with a protective effect in the FTND score analysis, while rs9285875 is associated with risk for higher FTND scores. The table contains uncorrected p-values, where significant p- values are bolded and underlined. No markers survived correction for multiple testing. Significant Q p-values are italicized. SNP, single nucleotide polymorphism; the Allele column represents the minor allele; Q p-values represent Cochrane’s Q-statistic p-values.