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. 2011 Sep 22;7(9):e1002260. doi: 10.1371/journal.pgen.1002260

Figure 7. Novel loci identified in this study placed in the context of previously confirmed CAD loci.

Figure 7

Previously reported variants listed are those from the NHGRI GWA studies catalogue [32] reported as having P<5×10−8 with CAD. Per-allele odds ratios and percentage risk allele frequencies (‘Freq’) are those listed in the catalogue. Frequencies and per-allele odds ratios for the novel variants reported in this study (appearing below the dashed line) are from the CARDIoGRAM replication stage.