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. Author manuscript; available in PMC: 2014 Feb 1.
Published in final edited form as: Eur J Neurol. 2012 Aug 6;20(2):300–308. doi: 10.1111/j.1468-1331.2012.03846.x

Table 2.

SNP information and reason for inclusion

SNP information Reason for inclusion in current study
SNP Chromosome Position (bp)a Gene or bNearest gene Associated Disease Reference(s)
rs646776c 1p13 109818530 CELSR2-PSRC1-SORT1b MI 20
rs11206510c 1p32 55496039 PCSK9b MI 20
rs6725887c 2q33 203745885 WDR12 MI 20
rs9818870 c 3q22 138122122 MRAS CAD 21
rs12526453 c 6p24 12927544 PHACTR1 MI 20
rs6922269 6q25 151252985 MTHFD1L CAD 22
rs2048327 6q25 160863532 SLC22A3 CAD 23
rs3127599 6q25 160907134 LPAL2 CAD 23
rs7767084 6q25 160962503 LPA CAD 23
rs10755578 6q25 160969738 LPA CAD 23
rs1333040 9p21 22083404 CDKN2BASb CAD, MI 22, 24, 25, 26
rs4977574 c 9p21 22098574 CDKN2BASb CAD, MI 22, 24, 25, 26
rs1333042 9p21 22103813 CDKN2BASb CAD, MI 22, 24, 25, 26
rs2383207 9p21 22115959 CDKN2BASb CAD, MI 22, 24, 25, 26
rs1746048 c 10q11 44775824 CXCL12b MI 20
rs2259816 12q24 121435587 HNF1A-C12orf43b CAD 21
rs1048990 14q13 35761675 PSMA6 MI 27, 28, 29
rs17228212 15q22 67458639 SMAD3 CAD 22
rs1122608 c 19p13 11163601 LDLRb MI 20
rs9982601 c 21q22 35599128 SLC5A3-MRPS6-KCNE2b MI 20
a

Chromosomal positions based on the February 2009 (GRCH37/hg19) genome assembly.

c

SNP examined in Cheng et al. [15].

CAD=coronary artery disease. MI=myocardial infarction.