Table 1.

Sequence Variants Used to Define Haplotypes in the LPL Locus. From Nickerson et al. (1998).

Sitea	Positionb	Variantc
1	106	C→A
2	110	A→C
3	145	G→A
4	325	T→C
5	343	(TG)3→(TG)4
6	479	T→C
7	551	(A)3→(A)2
8	736	T→C
9	1216	C→G
10	1220	T→C
11	1286	C→T
12	1547	A→C
13	1571	C→G
14	1828	C→G
15	1939	A→G
16	2131	C→T
17	2500	G→A
18	2619	A→G
19	2987	T→G
20	2996	C→A
21	3022	G→A
22	3248	C→G
23	3290	(T)7→(T)8
24	3297	(A)4→(A)5
25	3609	T→C
26	3723	T→C
27	3843	G→A
28	4016	C→G
29	4343	A→T
30	4346	C→G
31	4418	C→T
32	4426	T→C
33	4509	T→C
34	4576	A→T
35	4872	G→A
36	4935	T→C
37	5085	G→A
38	5168	T→C
39	5395	(A)8→(A)9
40	5441	T→C
41	5554	A→C
42	5560	A→G
43	5687	T→C
44	6250	C→T
45	6595	G→C
46	6678	T→G
47	6718	A→G
48	6772	A→G
49	6863	C→T
50	6939	delAAAT
51	7315	G→C
52	7344	A→G
53	7360	A→G
54	7413	T→C
55	7754	A→C
56	8088	insAG
57	8089	G→T
58	8285	C→G
59	8292	A→C
60	8393	T→G
61	8533	A→C
62	8537	A→C
63	8538	(A)3→(A)2
64	8644	T→C
65	8755	G→A
66	8852	T→G
67	9402	A→G
68	9712	G→A
69	9721	G→A

^aSite number assigned to each variable character used to define haplotypes in order, 5′ to 3′.

^bPosition in the baseline sequence (Genbank accession number AF050163).

^cSubstitution and insertion/deletion variants are reported as the state in the baseline sequence → alternative state.