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. 2019 Jul 10;7(8):e846. doi: 10.1002/mgg3.846

Table 2.

The genotypes frequency of all 16 studied variants in stroke cases and control subjects

Gene and variants Controls (n = 1,263) Stroke cases
Total cases (n = 1,405) Hemorrhagic stroke (n = 383) Atherothrombotic stroke (n = 607) Lacunar infarction (n = 415)
APOA1 PNTR
LRN 125 (9.9%) 1709 (12.1%) 48 (12.5%) 73 (12.0%) 49 (11.8%)
HRN 1,138 (90.1%) 1,235 (87.9%) 335 (87.5%) 534 (88.0%) 366 (88.2%)
MTHFR rs1801133
CC 410 (32.5%) 412 (29.3%) 116 (30.3%) 173 (28.5%) 123 (29.6%)
CT 585 (46.3%) 664 (47.3%) 182 (47.5%) 287 (47.3%) 195 (47.0%)
TT 268 (21.2%) 329 (23.4%) 85 (22.2%) 147 (24.2%) 97 (23.4%)
VKORC1 rs2359612
TT 1,099 (87.0%) 1,129 (80.4%) 314 (82.0%) 496 (81.7%) 319 (76.9%)
TC 156 (12.4%) 259 (18.4%) 62 (16.2%) 107 (17.6%) 90 (21.7%)
CC 8 (0.6%) 17 (1.2%) 7 (1.8%) 4 (0.7%) 6 (1.4%)
ALOX5AP rs4769874
GG 1,162 (92.0%) 1,277 (90.9%) 350 (91.4%) 551 (90.8%) 376 (90.6%)
GA 96 (7.6%) 122 (8.7%) 32 (8.4%) 52 (8.6%) 38 (9.2%)
AA 5 (0.4%) 6 (0.4%) 1 (0.3%) 4 (0.7%) 1 (0.2%)
ALOX5AP rs10507391
TT 635 (50.3%) 703 (50.0%) 205 (53.5%) 283 (46.6%) 215 (51.8%)
TA 505 (40.0%) 568 (40.4%) 145 (37.9%) 257 (42.3%) 166 (40.0%)
AA 123 (9.7%) 134 (9.5%) 33 (8.6%) 67 (11.0%) 34 (8.2%)
NOTCH3 rs1043994
GG 1,027 (81.3%) 1,169 (83.2%) 317 (82.8%) 502 (82.7%) 350 (84.3%)
GA 218 (17.3%) 211 (15.0%) 62 (16.2%) 94 (15.5%) 55 (13.3%)
AA 18 (1.4%) 25 (1.8%) 4 (1.0%) 11 (1.8%) 10 (2.4%)
VEGFA rs2010963
GG 386 (30.6%) 436 (31.0%) 135 (35.2%) 190 (31.3%) 111 (26.7%)
GC 619 (49.0%) 684 (48.7%) 179 (46.7%) 288 (47.4%) 217 (52.3%)
CC 258 (20.4%) 285 (20.3%) 69 (18.0%) 129 (21.3%) 87 (21.0%)
VEGFA rs1570360
GG 357 (28.3%) 401 (28.5%) 123 (32.1%) 166 (27.3%) 112 (27.0%)
GA 628 (49.7%) 709 (50.5%) 184 (48.0%) 300 (49.4%) 225 (54.2%)
AA 278 (22.0%) 295 (21.0%) 76 (19.8%) 141 (23.2%) 78 (18.8%)
VEGFA rs833061
TT 561 (44.4%) 616 (43.8%) 156 (40.7%) 266 (43.8%) 194 (46.7%)
TC 566 (44.8%) 628 (44.7%) 176 (46.0%) 273 (45.0%) 179 (43.1%)
CC 136 (10.8%) 161 (11.5%) 51 (13.3%) 68 (11.2%) 42 (10.1%)
KDR rs2071559
TT 624 (49.4%) 713 (50.7%) 168 (43.9%) 342 (56.3%) 203 (48.9%)
TC 505 (40.0%) 567 (40.4%) 175 (45.7%) 219 (36.1%) 173 (41.7%)
CC 134 (10.6%) 125 (8.9%) 40 (10.4%) 46 (7.6%) 39 (9.4%)
KDR rs1870377
AA 473 (37.5%) 519 (36.9%) 115 (30.0%) 249 (41.0%) 155 (37.3%)
AT 573 (45.4%) 632 (45.0%) 192 (50.1%) 254 (41.8%) 186 (44.8%)
TT 217 (17.2%) 254 (18.1%) 76 (19.8%) 104 (17.1%) 74 (17.8%)
Chr.9p21.3 rs2383206
AA 390 (30.9%) 417 (29.7%) 106 (27.7%) 170 (28.0%) 141 (34.0%)
AG 631 (50.0%) 674 (48.0%) 187 (48.8%) 289 (47.6%) 198 (47.7%)
GG 242 (19.2%) 314 (22.3%) 90 (23.5%) 148 (24.4%) 76 (18.3%)
Chr.9p21.3 rs2383207
AA 171 (13.5%) 192 (13.7%) 59 (15.4%) 72 (11.9%) 61 (14.7%)
AG 591 (46.8%) 629 (44.8%) 155 (40.5%) 280 (46.1%) 194 (46.7%)
GG 501 (39.7%) 584 (41.6%) 169 (44.1%) 255 (42.0%) 160 (38.6%)
Chr.9p21.3 rs10757278
AA 303 (24.0%) 312 (22.2%) 75 (19.6%) 132 (21.7%) 105 (25.3%)
AG 633 (50.1%) 658 (46.8%) 184 (48.0%) 274 (45.1%) 200 (48.2%)
GG 327 (25.9%) 435 (31.0%) 124 (32.4%) 201 (33.1%) 110 (26.5%)
Chr.9p21.3 rs10757274
AA 364 (28.8%) 378 (26.8%) 89 (23.2%) 158 (26.0%) 131 (31.6%)
AG 642 (50.8%) 667 (47.5%) 186 (48.6%) 284 (46.8%) 197 (47.5%)
GG 257 (20.3%) 360 (25.6%) 108 (28.2%) 165 (27.2%) 87 (21.0%)

Abbreviations: ALOX5AP, arachidonate 5‐lipoxygenase‐activating protein; APOA1, apolipoprotein (a); Chr.9p21.3, Chromosome 9p21.3; HRN, high repeat number (sum of both alleles ≥16); KDR, kinase insert domain‐containing receptor; LRN, low repeat number (sum of both alleles <16); MTHFR, methylenetetrahydrofolate reductase; PNTR, a pentanucleotide TTTTA repeat; VEGFA, vascular endothelial growth factor; VKORC1, vitamin K epoxide reductase complex subunit 1.