"Table 29.2. List of significantly associated haplotypes based on the ADHD GWS results using the Quebec Founder Population (QFP). Individual haplotypes with associated relative risks are presented in each row of the table; these values were extracted from the associated marker haplotype window with the most significant p value for each SNP in Table 29.1. The first column lists the region ID as presented in Table 1. The Haplotype column lists the specific nucleotides for the individual SNP alleles contributing to the haplotype reported. The Case and Control columns correspond to the numbers of cases and controls, respectively, containing the haplotype variant noted in the Haplotype column. The Total Case and Total Control columns list the total numbers of cases and controls for which genotype data was available for the haplotype in question. The RR column gives to the relative risk for each  particular haplotype. The remainder of the columns lists the SeqIDs for the SNPs contributing to the haplotype and their relative location with respect to the central marker. 
The Central marker (0) column lists the SeqID for the central marker on which the haplotype is based. 
Flanking markers are identified by minus (-) or plus (+) signs to indicate the relative location of flanking SNPs. "							
							
Region	Haplotype	Case	Control	TotalCase	TotalControl	RR	Central Marker (0)
762		C	119	143	354		354		0.750	21938
762		T	235	211	354		354		1.340	21938
762		G	176	138	354		354		1.550	21939
762		A	178	216	354		354		0.650	21939
762		C	78	65	354		354		1.260	21940
762		T	276	289	354		354		0.800	21940
762		C	307	258	354		354		2.430	21941
762		A	47	96	354		354		0.410	21941
762		A	116	146	354		354		0.690	21942
762		G	238	208	354		354		1.440	21942
762		G	146	119	354		354		1.390	21943
762		A	208	235	354		354		0.720	21943
762		G	185	161	354		354		1.310	21944
762		A	169	193	354		354		0.760	21944
