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. 2018 Sep 7;15(4):984–987. doi: 10.1016/j.jor.2018.08.042

Table 2.

Distribution of MTHFR 677C > T and 1298A > C genotypes and allelic frequencies in LCPD patients and control subjects.

Genotypes Cases (n = 45) Control (n = 55) OR (95% CI) P-value
MTHFR 677C > T
Genotype
CC 27 (60.0) 34 (61.8) Ref.
CT 15 (33.3) 19 (34.6) 0.947 (0.412–2.178) 0.899
TT 3 (6.7) 2 (3.6) 1.893 (0.302–11.852) 0.495
Allele
C 69 (76.7) 87 (79.1) 0.869 (0.444–1.699) 0.681
T 21 (23.3) 23 (20.9) 0.946 (0.474–1.888) 0.874
Dominant (TT + CT vs. CC) 1.079 (0.482–2.420) 0.853
Recessive (TT vs. CT + CC) 1.893 (0.302–11.852) 0.495
MTHFR 1298A > C
Genotype
AA 23 (51.1) 30 (54.5) Ref.
AC 20 (44.5) 24 (43.7) 1.033 (0.467–2.285) 0.935
CC 2 (4.4) 1 (1.8) 2.512 (0.220–28.634) 0.458
Allele
A 66 (73.3) 84 (76.4) 0.851 (0.448–1.617) 0.651
C 24 (26.7) 26 (23.6) 1.175 (0.618–2.232) 0.623
Dominant (TT + CT vs. CC) 1.148 (0.521–2.528) 0.732
Recessive (TT vs. CT + CC) 2.512 (0.220–28.634) 0.458

OR: Odds Ratio; CI: Confidence Interval.