| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1204056923 | 1.000 | 0.040 | 2 | 178590160 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs121913368 | 0.925 | 0.040 | 7 | 140753345 | missense variant | AG/GA | mnv | 1 | |||
| rs1238066548 | 1.000 | 0.040 | 19 | 38595699 | missense variant | G/A;T | snv | 1 | |||
| rs1277219458 | 1.000 | 0.040 | 2 | 241143002 | missense variant | C/T | snv | 1 | |||
| rs1451501407 | 1.000 | 0.040 | 17 | 8006628 | missense variant | G/A | snv | 1 | |||
| rs1458591077 | 1.000 | 0.040 | 2 | 178630352 | missense variant | C/T | snv | 1 | |||
| rs1484691555 | 1.000 | 0.040 | 20 | 9539512 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs267599092 | 1.000 | 0.040 | 2 | 178779043 | missense variant | C/T | snv | 1 | |||
| rs267600891 | 1.000 | 0.040 | 6 | 166469882 | missense variant | C/T | snv | 1 | |||
| rs267601046 | 1.000 | 0.040 | 6 | 43283303 | missense variant | C/T | snv | 1 | |||
| rs267601191 | 1.000 | 0.040 | 7 | 100819817 | missense variant | G/A | snv | 1 | |||
| rs267605306 | 1.000 | 0.040 | 19 | 14446504 | missense variant | C/G;T | snv | 1.6E-05 | 1 | ||
| rs369098292 | 1.000 | 0.040 | 2 | 178572742 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs374713701 | 1.000 | 0.040 | 2 | 178593660 | missense variant | C/A;T | snv | 4.0E-06; 8.1E-06 | 1 | ||
| rs375422359 | 1.000 | 0.040 | 2 | 178563634 | missense variant | C/T | snv | 2.4E-05 | 3.5E-05 | 1 | |
| rs55735910 | 1.000 | 0.040 | 8 | 47881444 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
| rs564777385 | 1.000 | 0.040 | 2 | 178800635 | missense variant | C/G;T | snv | 3.6E-05 | 1 | ||
| rs764005465 | 1.000 | 0.040 | 2 | 178572808 | missense variant | C/T | snv | 8.1E-06 | 1 | ||
| rs779173667 | 1.000 | 0.040 | 4 | 54290418 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 1 | |
| rs868224085 | 1.000 | 0.040 | 2 | 221482474 | missense variant | G/A | snv | 1 | |||
| rs907102077 | 1.000 | 0.040 | 3 | 9760752 | missense variant | G/A | snv | 1 | |||
| rs993022333 | 0.851 | 0.080 | 4 | 54733173 | missense variant | A/C;T | snv | 2 | |||
| rs104894095 | 0.827 | 0.120 | 9 | 21971200 | missense variant | C/G;T | snv | 9.0E-06 | 3 | ||
| rs121913378 | 0.776 | 0.280 | 7 | 140753337 | missense variant | C/A;G;T | snv | 6 | |||
| rs121913227 | 0.653 | 0.320 | 7 | 140753336 | missense variant | AC/CT;TT | mnv | 1 |