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Chunk #29 — Results — Associations of CD with the positive variants identified in the EA family sample in the other three independent samples

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Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample.
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In subjects carrying the SNP3^G allele, the frequency of SNP8^T/T in CD cases was significantly higher than controls (P=0.008, OR=1.8, 95%CI: 1.1~ 2.9), while no significant difference was observed within subjects not carrying SNP3^G. On the other hand, in CD subjects carrying SNP8^T/T, the frequency of SNP3^G+ was nominally higher than in controls (P=0.024, OR=1.6, 95%CI: 1.0~2.4), but no difference was observed within subjects not carrying SNP8^T/T (P>0.05) (Table 4, Figure 4).