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. 2019 Jul-Aug;51(4):248–254. doi: 10.4103/ijp.IJP_215_19

Table 4.

Allelic frequency of methylenetetrahydrafolate reductase C677T and A1298C polymorphism in control, deep vein thrombosis and coronary artery disease patients

MTHFR polymorphism Control (n=120), n (%) DVT (n=120), n (%) CAD (n=120), n (%) Crude ORa (95% CI) Crude ORb (95% CI)
MTHFR6C77T
 C/C 104 (86.67) 91 (75.83) 88 (73.33) 1.0 (reference) 1.0 (reference)
 C/T 15 (12.50) 25 (20.83) 29 (24.17) 1.90 (0.95-3.83) 2.28* (1.15-4.53)
 T/T 1 (0.83) 4 (3.33) 3 (2.50) 4.57 (0.50-41.66) 3.54 (0.36-34.71)
 CT + TT 16 (13.33) 29 (24.16) 32 (26.67) 2.07* (1.06-4.06) 2.36* (1.22-4.59)
Allele frequency
 C 0.93 0.86 0.85
 T 0.07 0.14 0.15
MTHFR A1298C
 AA 49 (40.83) 55 (45.83) 58 (48.33) 1.0 (reference) 1.0 (reference)
 AC 68 (56.67) 51 (42.50) 54 (45.00) 0.67 (0.39-1.13) 0.67 (0.40-1.13)
 CC 3 (2.50) 14 (11.67) 8 (6.67) 4.16* (1.13-15.34) 2.25 (0.57-8.96)
 AC + CC 71 (59.17) 65 (54.17) 62 (51.67) 0.81 (0.49-1.36) 0.74 (0.44-1.23)
Allele frequency
 A 0.69 0.67 0.71
 C 0.31 0.33 0.29

*P<0.05 as compared to reference genotype using Chi-square analysis, aOR=OR for DVT and, bOR=OR for CAD. OR=Odd ratio, CI=Confidence interval, DVT=Deep vein thrombosis, CAD=Coronary artery disease, MTHFR=Methylenetetrahydrafolate reductase