Table 3.
MTHFR A1298C (1801131)a 481/168/20b |
MTHFR C677T (1801133) 487/165/18 |
MTRR A66G (1801394) 461/183/25 |
MCP1 A2518G (1024611) 477/172/19 |
BHMT G742A (3733890) 481/172/17 |
TCN2 C777G (1801198) 473/165/30 |
SHMT C1420T (1979277) 479/172/18 |
NOS3 G894T (179983) 469/179/19 |
|
---|---|---|---|---|---|---|---|---|
R1c (95% CI) | 0.84 (0.68–1.04) | 1.22 (0.98–1.52) | 0.84 (0.64–1.09) | 1.02 (0.82–1.27) | 0.96 (0.77–1.19) | 0.77 (0.62–0.97) | 1.12 (0.9–1.4) | 1.03 (0.83–1.29) |
R2 (95% CI) | 0.91 (0.63–1.33) | 1.17 (0.82–1.66) | 0.79 (0.56–1.09) | 1.05 (0.68–1.61) | 0.86 (0.58–1.28) | 0.73 (0.52–1.02) | 1.22 (0.83–1.79) | 0.96 (0.65–1.41) |
S1d (95% CI) | 1.04 (0.82–1.31) | 1.15 (0.90–1.47) | 1.23 (0.90–1.69) | 0.99 (0.78–1.27) | 0.81 (0.64–1.04) | 1.17 (0.91–1.51) | 0.84 (0.66–1.08) | 1.26 (0.98–1.63) |
S2 (95% CI) | 0.83 (0.55–1.27) | 1.46 (1.01–2.12) | 1.17 (0.84–1.64) | 0.89 (0.55–1.44) | 0.84 (0.55–1.28) | 0.99 (0.71–1.37) | 0.67 (0.43–1.05) | 1.43 (0.94–2.20) |
LRT for offspring effects (p-value) | 2.59 (0.27) | 3.23 (0.20) | 2.24 (0.33) | 0.05 (0.97) | 0.56 (0.76) | 5.35 (0.07) | 1.43 (0.49) | 0.23 (0.89) |
LRT for maternal effects (p-value) | 0.97 (0.61) | 4.34 (0.11) | 1.66 (0.44) | 0.23 (0.89) | 2.97 (0.23) | 1.92 (0.38) | 3.99 (0.14) | 4.77 (0.09) |
dbSNP rs#
Number of triads with genotype data for 3, 2 or 1 member.
R1 and R2 denote the relative risk to cases with the heterozygous and rare homozygous genotypes, respectively, as compared to cases with the common homozygous genotype.
S1 and S2 denote the relative risk to offspring of women with the heterozygous and rare homozygous genotypes, respectively, as compared to the common homozygous genotype.