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. 2021 Sep 22;2021:5542292. doi: 10.1155/2021/5542292

Table 2.

Allelic and genotypic frequency of maternal RNLS rs10887800 and rs2576178 polymorphisms in IS patients and control group.

IS (N = 154) Control (N = 165) P value OR (95% CI)
RNLS rs10887800
Codominant
AA, n (%) 41 (26.6) 57 (34.5) 1
AG, n (%) 88 (57.1) 75 (45.5) 0.054 1.7 (1-2.7) 0.058
GG, n (%) 25 (33) 33 (20) 0.894 1.1 (0.5-2) 0.878
Dominant (AG + GG vs. AA) 0.122 1.5 (0.9-2.4) 0.126
Recessive (GG vs. AG + AA) 0.363 0.8 (0.4-1.4) 0.385
Overdominant (AG vs. AA+ GG) 0.033 1.6 (1-2.5) 0.037
Allele
 A, n (%) 170 (55) 189 (57) 1
 G, n (%) 138 (45) 141 (43) 0.632 1.1 (0.8-1.5)
RNLS rs2576178
AA, n (%) 115 (74.7) 115 (69.7) 1
AG, n (%) 32 (20.8) 42 (25.5) 0.306 0.8 (0.5-1.3) 0.313
GG, n (%) 7 (4.5) 8 (4.8) 0.756 0.9 (0.3-2.4) 0.803
Dominant model (AG + GG vs. AA) 0.307 0.8 (0.5-1.3) 0.323
Recessive model (GG vs. AG + AA) 0.855 0.9 (0.3-2.6) 0.899
Overdominant (AG vs. AA+GG) 0.321 0.8 (0.5-1.3) 0.324
Allele
A, n (%) 262 (85) 272 (82) 1
G, n (%) 46 (15) 58 (18) 0.392 0.8 (0.5-1.3)