| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
| rs2430561 | 0.590 | 0.760 | 12 | 68158742 | intron variant | T/A | snv | 0.36 | 50 | ||
| rs1444669684 | 0.658 | 0.480 | 9 | 21994285 | missense variant | C/A;T | snv | 36 | |||
| rs696 | 0.708 | 0.520 | 14 | 35401887 | 3 prime UTR variant | C/T | snv | 0.45 | 22 | ||
| rs2233406 | 0.732 | 0.440 | 14 | 35405593 | upstream gene variant | G/A | snv | 0.26 | 12 | ||
| rs1451506414 | 0.882 | 0.200 | 11 | 64598561 | synonymous variant | G/A | snv | 4 | |||
| rs10854554 | 0.925 | 0.080 | 22 | 19623159 | regulatory region variant | A/G | snv | 0.18 | 2 | ||
| rs62341639 | 0.925 | 0.080 | 4 | 184238281 | intergenic variant | C/T | snv | 0.20 | 2 | ||
| rs12457893 | 1.000 | 0.080 | 18 | 63258928 | intron variant | A/C | snv | 0.39 | 1 | ||
| rs1955656 | 1.000 | 0.080 | 14 | 94579038 | intron variant | G/A | snv | 0.14 | 1 | ||
| rs2093266 | 1.000 | 0.080 | 14 | 94566450 | intron variant | G/A | snv | 0.15 | 1 | ||
| rs62341657 | 1.000 | 0.080 | 4 | 184238385 | intergenic variant | G/A | snv | 0.18 | 1 | ||
| rs8094315 | 1.000 | 0.080 | 18 | 63268814 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs9617814 | 1.000 | 0.080 | 22 | 19622420 | regulatory region variant | A/G | snv | 0.22 | 1 | ||
| rs753482595 | 0.925 | 0.200 | 4 | 9920389 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 3 | |
| rs775020499 | 1.000 | 0.080 | 9 | 127467764 | missense variant | A/G | snv | 8.2E-06 | 1 | ||
| rs1370328347 | 1.000 | 0.080 | 17 | 63895621 | missense variant | C/A;T | snv | 1.0E-05; 1.0E-05 | 1 | ||
| rs782818582 | 0.882 | 0.160 | 9 | 133456116 | stop gained | C/T | snv | 1.2E-05 | 7.0E-06 | 3 | |
| rs767816037 | 1.000 | 0.080 | 17 | 63872725 | missense variant | C/G;T | snv | 4.5E-05 | 1 | ||
| rs121907896 | 0.851 | 0.200 | 11 | 64591825 | missense variant | G/A | snv | 1.8E-04 | 8.4E-05 | 5 | |
| rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
| rs121907892 | 0.807 | 0.240 | 11 | 64593747 | stop gained | G/A;C | snv | 2.8E-04 | 8 | ||
| rs561633150 | 0.925 | 0.200 | 4 | 9980627 | missense variant | C/T | snv | 6.1E-04 | 9.1E-05 | 2 | |
| rs1800777 | 0.724 | 0.280 | 16 | 56983407 | missense variant | G/A | snv | 3.7E-02 | 2.8E-02 | 17 | |
| rs1800471 | 0.597 | 0.840 | 19 | 41352971 | missense variant | C/G;T | snv | 5.6E-02 | 48 |