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. 2021 May 27;14:621–629. doi: 10.2147/PGPM.S303666

Table 2.

Distributions of Genotype and Allele Frequencies of SNPs rs2074192, rs2106809, rs1799752, rs4762, rs699 and rs5186 Observed in Asymptomatic and Symptomatic Patients

Asymptomatic (n=50) Symptomatic (n=54)
rs2074192
ACE2 (Xp22.2)
c.*1860-449C>T
intron variant
Genotypes (%) C/C 28 (56) 27 (50)
C/T 21 (42) 7 (13)
T/T 1 (2) 20 (37)
Alleles (%) C 77 (77) 61 (56)
T 23 (23) 47 (44)
HW (p) females 0.37 0.0088
HW (p) males 0.13 <0.0001
rs2106809
ACE2 (Xp22.2)
c.*264+788T>C
intron variant
Genotypes (%) A/A 38 (76) 40 (74)
A/G 4 (8) 3 (6)
G/G 8 (16) 11 (20)
Alleles (%) A 80 (80) 83 (77)
G 20 (20) 25 (23)
HW (p) females 0.27 0.076
HW (p) males <0.0001 <0.0001
rs1799752
ACE1 (17q23.3)
c.2306-117_2306-116ins-del
intron variant
Genotypes (%) I/I 22(44) 7(13)
I/D 21(42) 15(28)
D/D 7(14) 32(59)
Alleles (%) I 65(65) 29(27)
D 35 (35) 79(73)
HW (p) 0.55 0.037
rs4762
AGT (1q42.2)
c.620C>T
p.Thr207Met
Genotypes (%) C/C 35 (70) 38 (70)
C/T 14 (28) 16 (30)
T/T 1 (2) 0 (0)
Alleles (%) C 84 (84) 92 (85)
T 16 (16) 16 (15)
HW (p) 1 0.58
rs699
AGT (1q42.2)
c.803T>C
p.Met268Thr
Genotypes (%) T/T 19 (38) 17 (31)
T/C 31 (62) 25 (46)
C/C 0 (0) 12 (22)
Alleles (%) T 69 (69) 59 (55)
C 31 (31) 49 (45)
HW (p) 0.0018 0.59
rs5186
AGTR1 (3q24)
p.Met268Thr
3ʹ Prime UTR Variant
Genotypes (%) A/A 27 (54) 35 (65)
A/C 21 (42) 17 (31)
C/C 2 (4) 2 (4)
Alleles (%) A 75 (75) 87 (81)
C 25 (25) 21 (19)
HW (p) 0.7 1

Notes: For each polymorphism the relative gene, chromosomal position, nucleotide variant and amino acid consequence are described.

Abbreviations: D, deletion; HWE, Hardy–Weinberg equilibrium; I, insertion.