Table 3.
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.