Table 4. . Results of three case–control association tests.

(A) Genotype test
Rank	SNP	Gene	Chr	Location	Stat	p0	p-value
1	rs3136541	GAL	11	Intronic	11.815	0.0028	0.2457
2	rs2271933	HCRTR1	1	Missense variant	9.1702	0.0081	0.6628
3	s33933482	AVPR1B	1	3′-UTR	9.0174	0.0127	0.6938
4	rs1893679	GAL	11	2KB upstream	8.7719	0.013	0.7298
5	rs4518200	NPY1R	4	Intronic	7.3525	0.0457	0.9231
6	rs973002	CRHR2	7	Intronic	7.1004	0.0335	0.9420
7	rs2270007	CRHR2	7	Intronic	7.0992	0.0337	0.9421
8	rs1715747	CRHBP	5	Intronic	6.6137	0.0345	0.9721
9	rs4691075	NPY1R	4	Intronic	6.2724	0.0459	0.9848
10	rs4691910	NPY1R	4	Intronic	6.2724	0.0459	0.9848
(B) F-test
Rank	SNP	Gene	Chr	Location	Stat	p0	p-value
1	rs3136541	GAL	11	Intronic	10.4347	0.0021	0.1668
2	s33933482	AVPR1B	1	3′-UTR	8.8989	0.0060	0.3495
3	rs1893679	GAL	11	2KB upstream	8.7190	0.0095	0.3755
4	rs1715747	CRHBP	5	Intronic	6.6137	0.0372	0.7865
5	rs4518200	NPY1R	4	Intronic	6.4694	0.0266	0.8092
6	rs4691075	NPY1R	4	Intronic	6.0371	0.0386	0.8747
7	rs4691910	NPY1R	4	Intronic	6.0371	0.0386	0.8747
8	rs1500	CRHBP	5	Noncoding transcript	5.7612	0.0586	0.9102
9	rs2271933	HCRTR1	1	Missense variant	5.7603	0.0293	0.9105
10	rs1056526	HCRTR1	1	Synonymous	5.1361	0.0561	0.9690
(C) Maximum test
Rank	SNP	Gene	Chr	Location	Stat	p0	p-value
1	rs3136541	GAL	11	Intronic	11.5906	0.0017	0.1180
2	s33933482	AVPR1B	1	3′-UTR	8.6916	0.0063	0.4829
3	rs1893679	GAL	11	2KB upstream	8.6124	0.0082	0.4902
4	rs2270007	CRHR2	7	Intronic	7.0954	0.0189	0.7783
5	rs973002	CRHR2	7	Intronic	7.0589	0.0223	0.7842
6	rs1715747	CRHBP	5	Intronic	6.4569	0.0234	0.8760
7	rs2271933	HCRTR1	1	Missense variant	5.7153	0.0347	0.9565
8	rs17339455	NR3C1	5	Intronic	5.6543	0.0491	0.9612
9	rs1500	CRHBP	5	Noncoding transcript	5.6251	0.0371	0.9631
10	rs1056526	HCRTR1	1	Synonymous	4.9800	0.0510	0.9880

SNPs are listed by Stat in descending order. Bold terms indicates p < 0.50.

Chr: Chromosome number; MAF: Minor allelic frequency; p0: Nominal significance level; Stat: Test statistic.