Table 2.
Chromosome Location | Gene | Risk SNP (Hets/Hom/#Typed) | Univariate Analysis (p-value) | Final Model (coefficient) | Final Model (p-value) | Haplotyping Results |
---|---|---|---|---|---|---|
4q31.23 | NR3C2 | rs3843413 22/94/121 |
0.065 | −0.524 | 0.007 | L-M* |
11q14.3 | GRM5† | rs1874946 100/35/237 |
0.015 | 1.000 | <0.0001 | L-T** |
11q23.2 | NCAM1 | rs1545086 127/40/240 |
0.052 | 0.644 | 0.004 | L-M*/L-T** |
11q23.2 | DRD2† | rs4587762 107/42/237 |
0.022 | 0.764 | 0.004 | L-M***/M-T***/L-T*** |
12q14.2 | AVPR1A† | rs10877970 63/9/236 |
0.051 | 0.699 | 0.003 | M-T* |
15q13.3 | CHRNA7 | rs1514246 105/26/236 |
0.076 | 0.515 | 0.005 | L-M**/M-T**/L-T** |
15q21.1 | SQRDL | rs626808 75/7/240 |
0.135 | 0.537 | 0.006 | M-T* |
16p13.2 | GRIN2A† | rs8047589 99/103/238 |
0.060 | 0.592 | 0.004 | L-M**/M-T**/L-T* |
Loci included in the Initial Model of the Latent genetic variable (see text).
See text for the full names of the genes and Supplemental Table 1 for a complete presentation of the information concerning each risk single nucleotide polymorphism (SNP). The reference SNP ID number (rs#) is provided as is the number of heterozygotes (HETs), the number of homozygotes (HOMs), as well as the total number of individuals typed for the identified risk alleles. L = Low; M = Middle; and T = Top refer to the low, middle and top scores on the latent antisocial variable (see Figure 2). The coefficient for NR3C2 has a negative sign indicating that the more frequently occurring genotype C is associated with an increased risk of antisocial behavior when considered in combination with the other genes.
p <0.05;
p <0.01;
p <0.001