Table 1.

Pair-wise Disequilibrium Between Candidate SNPs in CHRM2

	Gene Location
	Intron 3–4						Intron 4–5	Intron 5–6	3′UTR
Marker a	rs978437	rs36210735	rs7782965	rs7800170	rs1455858	rs1378646	rs1824024	rs324650	rs8191992
Location b	136264718	136274187	136274673	136274860	136282243	136285541	136294234	136344201	136351848
rs978437 (A=.70; G=.30) c		1.00	1.00	1.00	.94	.97	.94	.64	.78
rs36210735 (C=.55; T=.45)	.53		1.00	1.00	.92	.92	.90	.68	.80
rs7782965 (C=.71; T=.29)	.95	.50		1.00	.98	.98	.98	.67	.79
rs7800170 (A=.55; C=.45)	.52	.98	.49		.92	.92	.90	.68	.80
rs1455858 (A=.30; G=.70)	.88	.45	.93	.44		1.00	1.00	.64	.74
rs1378646 (A=.69; G=.31)	.91	.47	.89	.46	.95		.98	.63	.74
rs1824024 (G=.31; T=.69)	.87	.44	.90	.43	.97	.95		.65	.74
rs324650 (A=.55; T=.45)	.22	.45	.23	.46	.22	.22	.23		.79
rs8191992 (A=.56; T=.44)	.33	.61	.33	.61	.30	.31	.30	.60

Notes: UTR, untranslated region; A, adenine; C, cytosine; G, guanine; T, thymine; all SNPs were in Hardy-Weinberg equilibrium; D′ values are presented above the diagonal; R² values are presented below the diagonal.

^aMarkers are shown as rs numbers from the dbSNP database.

^bLocations are derived from estimates of chromosomal position in the dbSNP database (build 36.3), and are expressed in terms of base pairs.

^cMarker specific allele frequencies.