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. 2017 Aug 3;12(8):e0181308. doi: 10.1371/journal.pone.0181308

Table 8. Observed versus expected minor allele frequency for gene polymorphisms associated with statin myalgia in cases versus controls compared to population frequency.

Gene SNP ID
(Major/minor allele)
Cases MAF§
(N = 12)
Controls MAF
(N = 7)
Expected MAF
HAP MAP (CEU)
(N = 90)
Nominal P*
SLCO1B1 rs4149056 (C/T) 0.33 0.00 0.15 0.039
rs2306283 (C/T) 0.83 0.43 0.39 0.170
SLCO2B1 rs12422149 (G/A) 0.51 0.08 0.09 0.01
ABCC1 rs4148330 (A/G) 0.92 0.71 0.33 0.313
ABCB1 rs1128503 (C/T) 0.67 0.43 0.45 0.268
CoQ2 rs4693075 (C/G) 0.67 0.71 0.34 0.832
RYR2 rs2819742 (A/G) 1.00 0.57 0.40 0.016
HTR3B rs2276307 (A/G) 0.42 0.43 0.23 0.960
HTR7 rs1935349 (A/G) 0.17 0.29 0.12 0.832
rs1176744 (G/T) 0.50 0.57 0.25 0.908
GATM rs2453533 (A/C) 0.33 0.71 0.29 0.131
rs1145086 (A/C/G/T) 0.33 0.71 0.33 0.131

Data are risk allele frequency (%) for SNPs previously associated with statin myalgia and myositis in case control and population studies. MAF is shown for cases and controls along with expected frequency in a population representative of the cohort. Risk Allele is shown in Bold. Differences in allele frequency between cases vs controls were assessed using Chi Square analysis. Nominal P values (Pearson) are provided.

§ MAF = minor allele frequency.

Expected minor allele frequency in a European population (HAP-MAP CEU)

* difference in minor allele frequency between cases and controls was assessed by Student T-Test (unadjusted). Nominal p values are presented.