| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs222054 | 1.000 | 0.040 | 4 | 71738582 | downstream gene variant | C/G | snv | 0.27 | 1 | ||
| rs2276736 | 1.000 | 0.040 | 3 | 148708086 | intron variant | A/G;T | snv | 1 | |||
| rs2303861 | 1.000 | 0.040 | 11 | 44618466 | intron variant | A/G | snv | 0.73 | 1 | ||
| rs2306986 | 1.000 | 0.040 | 4 | 99583418 | missense variant | G/C;T | snv | 5.9E-02 | 1 | ||
| rs2668423 | 1.000 | 0.040 | 19 | 1370527 | intron variant | T/G | snv | 0.73 | 1 | ||
| rs2829145 | 1.000 | 0.040 | 21 | 24495924 | intron variant | G/A | snv | 0.11 | 1 | ||
| rs35929428 | 1.000 | 0.040 | 9 | 8485834 | missense variant | G/A;C | snv | 9.2E-02; 4.0E-06 | 1 | ||
| rs3743788 | 1.000 | 0.040 | 16 | 55700194 | missense variant | T/C | snv | 3.2E-03 | 9.6E-04 | 1 | |
| rs3772627 | 1.000 | 0.040 | 3 | 148712467 | intron variant | A/G | snv | 0.44 | 1 | ||
| rs3772630 | 1.000 | 0.040 | 3 | 148708685 | intron variant | T/C | snv | 0.44 | 1 | ||
| rs3772633 | 1.000 | 0.040 | 3 | 148700381 | intron variant | T/C | snv | 0.13 | 1 | ||
| rs3805335 | 1.000 | 0.040 | 4 | 99586478 | intron variant | C/T | snv | 1.3E-02 | 1 | ||
| rs3806622 | 1.000 | 0.040 | 3 | 57226802 | intron variant | C/G | snv | 0.47 | 1 | ||
| rs3810622 | 1.000 | 0.040 | 22 | 43942254 | intron variant | T/C;G | snv | 0.40 | 1 | ||
| rs4149267 | 1.000 | 0.040 | 9 | 104889664 | intron variant | T/C | snv | 0.47 | 1 | ||
| rs4686434 | 1.000 | 0.040 | 3 | 186647354 | intron variant | A/C;G | snv | 1 | |||
| rs497408 | 1.000 | 0.040 | 6 | 23993395 | regulatory region variant | C/A;T | snv | 1 | |||
| rs537635771 | 1.000 | 0.040 | 20 | 46128178 | missense variant | C/G;T | snv | 1 | |||
| rs5748926 | 1.000 | 0.040 | 22 | 17168884 | upstream gene variant | T/C | snv | 0.70 | 1 | ||
| rs5764455 | 1.000 | 0.040 | 22 | 44002644 | intron variant | A/C;G | snv | 1 | |||
| rs6006460 | 1.000 | 0.040 | 22 | 43946294 | missense variant | G/T | snv | 7.6E-03 | 3.1E-02 | 1 | |
| rs6006611 | 1.000 | 0.040 | 22 | 44004818 | intron variant | G/A | snv | 0.44 | 1 | ||
| rs6128907 | 1.000 | 0.040 | 20 | 38759219 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs61733139 | 1.000 | 0.040 | 4 | 99583409 | missense variant | G/C | snv | 4.0E-02 | 4.9E-02 | 1 | |
| rs61756425 | 1.000 | 0.040 | 8 | 9141529 | missense variant | G/T | snv | 1.6E-02 | 1.0E-02 | 1 |