| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 | |||
| rs77724903 | 0.672 | 0.280 | 10 | 43118460 | missense variant | A/G;T | snv | 4.0E-06; 2.1E-03 | 4 | ||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
| rs1400295986 | 0.925 | 0.080 | 5 | 112838233 | missense variant | T/C | snv | 2 | |||
| rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 2 | |||
| rs2066844 | 0.587 | 0.520 | 16 | 50712015 | missense variant | C/T | snv | 2.6E-02 | 2.9E-02 | 2 | |
| rs2066845 | 0.611 | 0.600 | 16 | 50722629 | missense variant | G/C;T | snv | 1.1E-02; 2.2E-04 | 2 | ||
| rs28933379 | 1.000 | 0.080 | 5 | 112838953 | missense variant | G/A | snv | 1 | |||
| rs372481703 | 1.000 | 0.080 | 5 | 112839106 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | |
| rs121909776 | 1.000 | 0.080 | 2 | 201187798 | missense variant | T/C | snv | 1.2E-04 | 2.8E-05 | 1 | |
| rs35187787 | 0.827 | 0.120 | 16 | 68822063 | missense variant | G/A;T | snv | 3.3E-03; 2.4E-05 | 1 | ||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs1800730 | 0.649 | 0.480 | 6 | 26090957 | missense variant | A/T | snv | 1.0E-02 | 1.0E-02 | 1 | |
| rs121912469 | 1.000 | 0.080 | 5 | 132489457 | missense variant | T/A | snv | 1 | |||
| rs121912470 | 0.925 | 0.120 | 5 | 132489448 | missense variant | A/G | snv | 1 | |||
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs104894361 | 0.882 | 0.240 | 12 | 25245370 | missense variant | T/A;C;G | snv | 4.0E-06 | 1 | ||
| rs121913528 | 0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv | 1 | |||
| rs28933369 | 0.925 | 0.080 | 17 | 39724744 | missense variant | G/A | snv | 1 | |||
| rs121908382 | 1.000 | 0.080 | 1 | 45331530 | missense variant | G/A | snv | 1 | |||
| rs121908383 | 1.000 | 0.080 | 1 | 45331502 | missense variant | T/C | snv | 1 | |||
| rs79777494 | 0.882 | 0.120 | 1 | 45334495 | missense variant | G/A | snv | 1.1E-03 | 4.9E-04 | 1 | |
| rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 1 | |
| rs367807476 | 1.000 | 0.080 | 19 | 1223035 | missense variant | C/G;T | snv | 9.2E-06 | 1.4E-05 | 1 | |
| rs202208566 | 1.000 | 0.080 | 12 | 109903156 | missense variant | T/C | snv | 6.5E-04 | 1.7E-04 | 1 |