Table 3.
Marker | OverallSignificancea | Significance ofHigh-RiskHaplotypeb |
rs490434 | … | … |
rs576666 | … | … |
rs531460 | .0066 | .000034 |
rs561779 | .0030 | .000075 |
rs495818 | .0064 | .000077 |
rs497068 | .0075 | .00010 |
rs572227 | .0037 | .000035 |
rs573400 | .0113 | .00050 |
rs541418 | .0088 | .0011 |
rs481311 | .0164 | .00010 |
rs507788 | .0127 | .00020 |
rs532780 | .0428 | .00070 |
rs548583 | .0028 | .000039 |
ss15649713 | .0258 | .00050 |
rs496650 | .0187 | .0010 |
rs540363 | .0427 | .0010 |
rs526752 | .0156 | .00020 |
rs530329 | .0060 | .00020 |
rs483160 | .0071 | .000084 |
rs279871 | .00010 | .000003 |
rs279867 | .000000 | .000001 |
rs279866 | .000003 | .000001 |
rs279863 | .00090 | .000004 |
rs279861 | .0052 | .000050 |
rs279858 | .0086 | .00030 |
rs175931 | .0030 | .00010 |
rs279843 | .0082 | .000096 |
rs279845 | .00080 | .000013 |
rs279846 | .0340 | .0014 |
rs183961 | .0042 | .000051 |
rs1440130 | .0018 | .000015 |
rs279826 | .0042 | .000061 |
ss15649712 | .0318 | .0062 |
rs279827 | .0240 | .0068 |
rs279828 | .0114 | .0029 |
rs279834 | .0141 | .000041 |
rs279836 | .0011 | .000004 |
rs279837 | .0025 | .000019 |
rs279841 | .0019 | .000023 |
rs189957 | .00080 | .000027 |
rs1442059 | .031 | .00020 |
rs1442061 | .022 | .0030 |
rs1442062 | .013 | .00010 |
ss15649712 | .026 | .00040 |
ss15649710 | .059 | .0040 |
rs3756007 | .35 | .0275 |
rs894269 | .15 | .0026 |
rs2165607 | .026 | .0023 |
rs1545234 | .24 | .0865 |
Note.— Each set of three consecutive SNPs through the GABRA2 gene was analyzed as an eight-allele marker, named by the third SNP in the set.
P value based on the average PDT (Martin et al. 2000), treating each haplotype as a marker in an eight-allele system; the value is shown at the third of the three SNPs used to create each haplotype.
Significance of the high-risk haplotype within each set of three consecutive SNPs.