| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6854845 | 0.827 | 0.080 | 4 | 74821455 | intergenic variant | G/T | snv | 0.13 | 6 | ||
| rs2853668 | 0.882 | 0.080 | 5 | 1299910 | upstream gene variant | G/T | snv | 0.33 | 5 | ||
| rs1525489 | 1.000 | 0.080 | 7 | 122993419 | downstream gene variant | A/G | snv | 3.6E-02 | 1 | ||
| rs17239025 | 1.000 | 0.080 | 13 | 30765768 | downstream gene variant | G/C | snv | 4.1E-02 | 1 | ||
| rs17268122 | 1.000 | 0.080 | 13 | 95192240 | intron variant | G/A;C;T | snv | 2 | |||
| rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 | |||
| rs12733285 | 0.776 | 0.120 | 1 | 202952912 | intron variant | C/T | snv | 0.26 | 12 | ||
| rs1342387 | 0.776 | 0.120 | 1 | 202945228 | intron variant | T/C | snv | 0.53 | 12 | ||
| rs4994 | 0.578 | 0.640 | 8 | 37966280 | missense variant | A/G | snv | 0.11 | 9.2E-02 | 65 | |
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs1126667 | 0.776 | 0.280 | 17 | 6999441 | missense variant | A/G | snv | 0.60 | 0.62 | 8 | |
| rs2073438 | 0.925 | 0.160 | 17 | 6996757 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs2619112 | 0.882 | 0.160 | 17 | 4632090 | intron variant | A/C;G | snv | 4.0E-06; 0.53 | 3 | ||
| rs776197565 | 0.827 | 0.120 | 5 | 112819214 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 39 | |
| rs1801673 | 0.882 | 0.120 | 11 | 108304736 | missense variant | A/T | snv | 4.9E-03 | 4.4E-03 | 3 | |
| rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
| rs2227935 | 0.925 | 0.080 | 15 | 90782869 | missense variant | C/A;G;T | snv | 4.0E-06; 5.6E-02 | 2 | ||
| rs2228545 | 1.000 | 0.080 | 2 | 202555989 | missense variant | G/A | snv | 2.4E-02 | 2.2E-02 | 1 | |
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
| rs2705535 | 1.000 | 0.080 | 3 | 112490080 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
| rs1801726 | 0.732 | 0.280 | 3 | 122284985 | missense variant | G/C | snv | 0.95 | 0.92 | 13 | |
| rs187115 | 0.695 | 0.320 | 11 | 35154612 | intron variant | T/C | snv | 0.37 | 22 | ||
| rs74790047 | 0.851 | 0.120 | 12 | 6601978 | missense variant | A/C;G | snv | 2.0E-05; 1.2E-04; 5.2E-03 | 1.7E-03 | 7 |