Table 2. The single nucleotide polymorphisms (SNPs) predictive of the subjects with 15% lowest and highest IMT levels in 2001.

SNP ID* (rs number)	Gene symbol (HGNC name)	SNP location (Chr region)	Significance† (p-value)	Predictive power‡ (%AUC)
rs2073658	USF1	1q23.3	0.70	11.8
rs1205	CRP	1q23.2	0.02	10.6
rs805305	DDAH2	6p21.33	0.38	9.68
rs3890182	ABCA1	9q31.1	0.81	7.53
rs6929137	C6orf97	6q25.1	0.10	7.53
rs4073307	IGSF1	Xq26.1	0.71	6.45
rs693	APOB	2p24.1	0.53	6.45
rs3130340	INTERGENIC	6p21.32	0.11	6.45
rs599839	PSRC1	1p13.3	0.10	6.45
rs754523	INTERGENIC	2p24.1	1.00	5.38
rs1143634	IL1B	2q13	0.51	5.38
rs4404254	ICOS	2q33.2	0.16	4.30
rs2548861	WWOX	16q23.1	0.14	4.30
rs2553268	WRN	8p12	0.15	3.23
rs4937100	IL18	11q23.1	0.22	2.15
rs2516839	USF1	1q23.3	0.13	2.15

*The SNPs identified also in the previous case-control association studies [9]–[21] are boldfaced.

†The corrected p-values larger than one were truncated to unity.

‡The SNPs are arranged according to their contribution to the overall prediction accuracy (AUC).