| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17132261 | 1.000 | 0.080 | 5 | 110672513 | intron variant | C/T | snv | 4.8E-02 | 2 | ||
| rs2292462 | 1.000 | 0.080 | 15 | 84657523 | intron variant | G/C;T | snv | 2 | |||
| rs768079285 | 1.000 | 0.080 | 10 | 20840824 | frameshift variant | T/- | delins | 8.0E-06 | 2 | ||
| rs10500279 | 1.000 | 0.080 | 19 | 38544428 | intron variant | G/C | snv | 5.6E-02 | 1 | ||
| rs1178625972 | 1.000 | 0.080 | 22 | 39966117 | missense variant | C/G | snv | 2.4E-05 | 1.4E-05 | 1 | |
| rs17168525 | 1.000 | 0.080 | 7 | 135928514 | 3 prime UTR variant | G/A | snv | 1.4E-02 | 1 | ||
| rs1957757 | 1.000 | 0.080 | 14 | 61730230 | intron variant | T/C | snv | 0.74 | 1 | ||
| rs1974201 | 1.000 | 0.080 | 6 | 131889981 | intron variant | G/A;C;T | snv | 1 | |||
| rs2071090 | 1.000 | 0.080 | 19 | 38524814 | intron variant | T/C | snv | 0.15 | 1 | ||
| rs2278239 | 1.000 | 0.080 | 5 | 79737483 | missense variant | A/C;G | snv | 0.14; 2.8E-05 | 1 | ||
| rs238234 | 1.000 | 0.080 | 17 | 4980523 | missense variant | C/A;G;T | snv | 5.6E-05; 0.75; 8.1E-06 | 1 | ||
| rs2960321 | 1.000 | 0.080 | 19 | 38557523 | intron variant | C/A | snv | 0.18 | 1 | ||
| rs4129218 | 1.000 | 0.080 | 12 | 65564881 | intron variant | G/A | snv | 0.70 | 1 | ||
| rs75404003 | 1.000 | 0.080 | 18 | 62361277 | intron variant | C/- | delins | 1 | |||
| rs756529 | 1.000 | 0.080 | 20 | 49394471 | intron variant | G/A | snv | 0.44 | 1 | ||
| rs9402349 | 1.000 | 0.080 | 6 | 131863968 | intron variant | A/C | snv | 9.8E-02 | 1 | ||
| rs9594782 | 1.000 | 0.080 | 13 | 42577050 | intron variant | T/C | snv | 4.0E-02 | 1 |