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. 2021 Oct 15;8:743868. doi: 10.3389/fcvm.2021.743868

Table 2.

Allelic and genotypic frequencies of the target RGMa promoter SNPs in enrolled patient group and healthy subject group.

CHS from 1,000 genome
(n = 108)
Enrolled patients group
(n = 201)
p -value
rs4778099 (allele and genotype frequency)
A 70 (32.4%) 131 (32.6%) 0.964
G 146 (67.6%) 271 (67.4)
AA 10 (9.3%) 23 (11.4%) 0.732
AG 50 (46.3%) 85 (42.3%)
GG 48 (44.4%) 93 (46.3%)
rs10520720 (allele and genotype frequency)
A 34 (15.7%) 63 (15.7%) 0.982
G 182 (84.3%) 339 (84.3%)
AA 2 (1.8%) 4 (2.0%) 0.994
AG 30 (27.8%) 55 (27.4%)
GG 76 (70.4%) 142 (70.6%)
rs725458 (allele and genotype frequency)
T 135 (62.5%) 247 (61.4%) 0.796
C 81 (37.5%) 155 (38.6%)
TT 43 (39.8%) 77 (38.3%) 0.965
TC 49 (45.4%) 93 (46.3%)
CC 16 (14.8%) 31 (15.4%)

CHS, Han population in Southern China.