Review Article
Effect of Polymorphisms in the FCN1, FCN2, and FCN3 Genes on the Susceptibility to Develop Rheumatoid Arthritis: A Systematic Review
Table 3
Allelic and genotypic frequencies of cases and controls.
| Study data | | Cases | Controls | Author | Year | Gene | RS | Alleles | Risk allele | Cases | Total alleles | Allele ref | Risk allele | WT | HT | HH | Control | Total alleles | Allele ref | Risk allele | WT | HT | HH |
| Addobbati C | 2015 | FCN1 | rs2989727 | C/T | T | 137 | 274 | 124 | 150 | 27 | 70 | 40 | 264 | 528 | 206 | 322 | 40 | 126 | 98 | rs1071583 | C/T | T | 137 | 274 | 165 | 109 | 50 | 65 | 22 | 264 | 528 | 341 | 187 | 109 | 123 | 132 | FCN2 | rs17514136 | A/G | G | 184 | 368 | 286 | 82 | 108 | 70 | 6 | 264 | 528 | 401 | 127 | 156 | 89 | 19 | rs3124954 | C/T | T | 184 | 368 | 241 | 127 | 84 | 73 | 27 | 264 | 528 | 345 | 183 | 116 | 113 | 35 | rs7851696 | G/T | T | 184 | 368 | 318 | 50 | 136 | 46 | 2 | 264 | 528 | 458 | 70 | 197 | 64 | 3 |
| Pieczarka C | 2020 | FCN1 | rs2989727 | G/A | A | 148 | 296 | 152 | 144 | 35 | 82 | 31 | 159 | 318 | 147 | 171 | 38 | 71 | 50 | rs10120023 | G/A | A | 148 | 296 | 230 | 66 | 89 | 52 | 7 | 159 | 318 | 224 | 94 | 74 | 76 | 9 | rs17039495 | G/A | A | 148 | 296 | 288 | 8 | 140 | 8 | 0 | 159 | 318 | 316 | 2 | 157 | 2 | 0 | rs10117466 | C/A | A | 148 | 296 | 234 | 62 | 93 | 48 | 7 | 159 | 318 | 232 | 86 | 81 | 70 | 8 | rs10858293 | G/T | T | 148 | 296 | 226 | 70 | 83 | 60 | 5 | 159 | 318 | 226 | 92 | 78 | 70 | 11 | FCN3 | rs532781899 | g.1637C/g.1637del | g.1637del | 148 | 296 | 290 | 6 | 142 | 6 | — | 160 | 320 | 312 | 8 | 153 | 7 | — | rs28362807 | g.3524_3532ins | g.3524_3532ins | 148 | 296 | 210 | 86 | 75 | 60 | 13 | 160 | 320 | 244 | 76 | 96 | 52 | 12 | rs4494157 | g.4473C/g.4473A | g.4473A | 148 | 296 | 215 | 81 | 79 | 57 | 12 | 160 | 320 | 250 | 70 | 102 | 46 | 12 |
| Vander Cruyssen B | 2007 | FCN1 | rs2989727 | G/A | A | 338 | 676 | 226 | 450 | 145 | 162 | 31 | 595 | 1190 | 476 | 714 | 220 | 268 | 107 | rs1071583 | A/G | G | 338 | 676 | 216 | 460 | 152 | 156 | 30 | 595 | 1190 | 464 | 726 | 226 | 274 | 95 | FCN2 | rs7865453 | A/C | C | 338 | 676 | 616 | 60 | — | — | — | 595 | 1190 | 1048 | 142 | — | — | — | rs32469537 | A/G | G | 338 | 676 | 480 | 196 | — | — | — | 595 | 1190 | 880 | 310 | — | — | — | rs17549193 | C/T | T | 338 | 676 | 466 | 210 | — | — | — | 595 | 1190 | 880 | 310 | — | — | — | rs7851696 | G/T | T | 338 | 676 | 608 | 68 | — | — | — | 595 | 1190 | 1036 | 154 | — | — | — | FCN3 | rs3813800 | C/G | G | 338 | 676 | 676 | 0 | — | — | — | 595 | 1190 | 1178 | 12 | — | — | — |
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WT: wild-type genotype or homozygous for the major allele; HT: heterozygous genotype; HH: genotype homozygous for the risk allele.
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