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. 2004 Jul 1;17(7):624–628. doi: 10.1016/j.amjhyper.2004.02.022

Table 3.

Genotype and allele frequencies of ACE2 polymorphisms in hypertensive (HT) and normotensive (NT) groups

Group n Genotype frequencies
Allele frequencies
MM Mm mm χ2 P M m χ2 P
Intron 1 A→G variant
 Female
  NT 81 55 (0.68) 25 (0.31) 1 (0.01) 2.9 0.23 135 (0.83) 27 (0.17) 1.1 0.31
  HT 78 50 (0.64) 23 (0.30) 5 (0.06) 123 (0.79) 33 (0.21)
 Male
  NT 96 * 68 (0.71) 28 (0.29) 0.28 0.60
  HT 48 36 (0.75) 12 (0.25)
Intron 3 G→A variant
 Female
  NT 89 63 (0.71) 20 (0.22) 6 (0.07) 1.9 0.39 146 (0.82) 32 (0.18) 0.89 0.35
  HT 65 40 (0.62) 21 (0.32) 4 (0.06) 101 (0.78) 29 (0.22)
 Male
  NT 104 * 83 (0.80) 21 (0.20) 0.52 0.47
  HT 46 39 (0.85) 7 (0.15)
Intron 11 C→G variant
 Female
  NT 89 23 (0.26) 50 (0.56) 16 (0.18) 2.2 0.33 96 (0.54) 82 (0.46) 1.9 0.17
  HT 100 34 (0.34) 54 (0.54) 12 (0.12) 122 (0.61) 78 (0.39)
 Male
  NT 89 * 62 (0.70) 27 (0.30) 0.0029 0.96
  HT 52 36 (0.69) 16 (0.31)
Intron 16 G→C variant
 Female
  NT 85 57 (0.67) 24 (0.28) 4 (0.05) 1.5 0.46 138 (0.81) 32 (0.19) 0.13 0.72
  HT 91 62 (0.68) 21 (0.23) 8 (0.09) 145 (0.80) 37 (0.20)
 Male
  NT 103 * 85 (0.83) 18 (0.17) 0.0017 0.95
  HT 47 39 (0.83) 8 (0.17)

M = major allele, m = minor allele, of each polymorphism.

Values in parentheses are fractions.

*

As ACE2 is on the X chromosome (one copy), it is inappropriate to present genotype data.