| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1617640 | 0.742 | 0.520 | 7 | 100719675 | upstream gene variant | C/A;G;T | snv | 15 | |||
| rs995922697 | 0.724 | 0.560 | 3 | 49357413 | missense variant | A/G | snv | 4.1E-06 | 15 | ||
| rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 14 | |||
| rs174594 | 0.776 | 0.160 | 11 | 61852357 | intron variant | C/A;T | snv | 14 | |||
| rs767830104 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 13 | ||
| rs1372834938 | 0.763 | 0.280 | 2 | 8812465 | missense variant | G/C | snv | 4.2E-06 | 12 | ||
| rs10887800 | 0.790 | 0.280 | 10 | 88316086 | intron variant | A/G;T | snv | 11 | |||
| rs28935197 | 0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 | 10 | ||
| rs1020608562 | 0.807 | 0.160 | 3 | 46373738 | missense variant | T/C | snv | 4.0E-06 | 9 | ||
| rs188942711 | 0.763 | 0.200 | 2 | 227253336 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 9 | ||
| rs756322971 | 0.763 | 0.240 | 3 | 122284955 | missense variant | C/A;G | snv | 9 | |||
| rs911119 | 0.807 | 0.120 | 20 | 23632100 | non coding transcript exon variant | C/G;T | snv | 9 | |||
| rs1801239 | 0.827 | 0.160 | 10 | 16877053 | missense variant | T/C;G | snv | 8.9E-02; 8.0E-06 | 8 | ||
| rs2229109 | 0.807 | 0.240 | 7 | 87550493 | missense variant | C/A;T | snv | 2.7E-02 | 8 | ||
| rs2229569 | 0.790 | 0.360 | 1 | 169704697 | missense variant | G/A;T | snv | 0.21; 3.2E-05 | 8 | ||
| rs2294021 | 0.776 | 0.280 | X | 49249149 | intron variant | T/A;C | snv | 0.52 | 8 | ||
| rs1394125 | 0.882 | 0.200 | 15 | 75866642 | intron variant | G/A;T | snv | 7 | |||
| rs881858 | 0.882 | 0.200 | 6 | 43838872 | intron variant | G/A;C | snv | 7 | |||
| rs12513649 | 0.851 | 0.160 | 5 | 173045049 | regulatory region variant | C/G;T | snv | 6 | |||
| rs7740107 | 1.000 | 0.080 | 6 | 130053316 | intron variant | T/A;G | snv | 6 | |||
| rs10951982 | 0.851 | 0.160 | 7 | 6382925 | intron variant | G/A;T | snv | 5 | |||
| rs149454410 | 0.925 | 0.120 | 4 | 9942000 | missense variant | C/G;T | snv | 4.0E-05; 3.2E-04 | 5 | ||
| rs186459505 | 0.925 | 0.120 | 3 | 52907083 | missense variant | G/A;T | snv | 1.1E-04; 4.0E-06 | 5 | ||
| rs28456 | 0.925 | 0.120 | 11 | 61822009 | intron variant | A/C;G | snv | 5 | |||
| rs7422339 | 1.000 | 0.080 | 2 | 210675783 | missense variant | C/A | snv | 5 |