Table 2.
Coronary artery disease: genetic loci with genome-wide significant association.
| Clinical coronary artery disease | ||||
|---|---|---|---|---|
| 1p13 (SORT1) rs602633*,# p=1×10−25 |
3q22 (MRAS) rs9818870 p=3×10−9 |
6q26 (PLG) rs4252120£ p=5×10−10 |
10q23 (LIPA) rs2246833 p=9×10−6 |
17p11 (PEMT) rs12936587 p=1×10−9 |
| 1p32 (PPAP2B) rs17114036 p=6×10−12 |
4q31 (EDNRA) rs1878406 p=3×10−8 |
7p21 (HDAC9) rs2023938 p=5×10−8 |
10q24 (CYP17A1) rs12413409¤ p=6×10−8 |
17p13 (SMG6) rs2281727 p=8×10−9 |
| 1p32 (PCSK9) rs11206510* p=2×10−5 |
4q32 (GUCY1A3) rs7692387¤ p=3×10−11 |
7q22 (COG5) rs12539895 p=5×10−4 |
11q22 (PGFD) rs974819 p=4×10−11 |
17q21 (GIP) rs15563£ p=9×10−6 |
| 1q21 (IL6R) rs4845625 p=4×10−10 |
5q31 (SLC22A4) rs273909 p=1×10−9 |
7q32 (ZC3HC1) rs11556924¤,£ p=7×10−17 |
11q23 (APOA1) rs9326246*,§,# p=2×10−7 |
19p13 (LDLR) rs1122608* p=6×10−14 |
| 1q41 (MIA3) rs17464857 p=6×10−5 |
6p21 (ANKS1A) rs12205331# p=4×10−5 |
8p21 (LPL) rs264§,# p=3×10−9 |
12q24 (SH2B3) rs3184504¤,#,&,£ p=5×10−11 |
19q13 (APOE) rs2075650*,§,# p=6×10−11 |
| 2p11 (VAMP8) rs1561198 p=1×10−10 |
6p21 (KCNK5) rs10947789 p=1×10−8 |
8q24 (TRIB1) rs2954029*,§,# p=5×10−9 |
13q12 (FLT1) rs9319428 p=7×10−11 |
21q22 (KCNE2) rs9982601 p=8×10−17 |
| 2p21 (ABCG5) rs6544713* p=2×10−9 |
6p24 (ADTRP) rs6903956 p=5×10−12 |
9p21 (CDKN2A/CDKN2B) rs1333049 p=1×10−52 |
13q34 (COL4A1-COL4A2) rs4773144 p=1×10−11 |
|
| 2p24 (APOB) rs515135* p=3×10−10 |
6p24 (PHACTR1) rs9369640 p=8×10−22 |
9q34 (ABO) rs579459* p=3×10−8 |
14q32 (HHIPL1) rs2895811 p=4×10−10 |
|
| 2q22 (ZEB2) rs2252641 p=5×10−8 |
6q23 (TCF21) rs12190287 p=5×10−13 |
10p11 (KIAA1462) rs2505083 p=1×10−11 |
15q25 (ADAMTS7) rs7173743 p=7×10−13 |
|
| 2q33 (WDR12) rs6725887£ p=1×10−15 |
6q25 (LPA) rs3798220* p=5×10−5 |
10q11 (CXCL12) rs501120 p=2×10−9 |
15q26 (FURIN) rs17514846¤ p=9×10−11 |
|
| Coronary artery calcium | ||||
| Chromosome | Candidate gene | SNP | P-value | |
| 6p24 | PHACTR1 | rs9349379 | p=3×10−11 | |
| 9p21 | CDKN2A/CDKN2B | rs1333049 | p=8×10−19 | |
Chromosomal loci, candidate genes, SNP and p-value at the 46 genetic loci associated with coronary artery disease in genome-wide association studies (p<5×10−8). Adapted from the CARDIoGRAMplusC4D study [18] (up to >60,000 cases and >130,000 controls) and a study of coronary artery calcium on computed tomography (nearly 16,000 subjects). [65] One locus (6p24 in ADTRP) was reported separately in a Chinese study. [48]
10 loci associated with higher LDL for CAD risk alleles,
1 locus with lower LDL,
4 loci with higher TG,
7 loci with lower HDL,
5 loci with higher blood pressure.,
5 coding variants with r2 > 0.9 to index SNP in 1000 Genomes CEU.