| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs63751612 | 0.925 | 0.120 | 3 | 37047520 | missense variant | A/G | snv | 1.2E-04 | 6.3E-05 | 2 | |
| rs63750217 | 0.807 | 0.240 | 3 | 37048955 | missense variant | G/A;C | snv | 2 | |||
| rs63750303 | 0.882 | 0.160 | 3 | 37014485 | missense variant | G/A;T | snv | 2 | |||
| rs63750449 | 0.925 | 0.120 | 3 | 37047640 | missense variant | A/C;G;T | snv | 3.5E-03; 8.4E-05 | 2 | ||
| rs121912965 | 0.882 | 0.200 | 3 | 36993651 | missense variant | TG/AC | mnv | 1 | |||
| rs63749838 | 0.925 | 0.160 | 3 | 36993620 | missense variant | A/G;T | snv | 1 | |||
| rs267607706 | 0.882 | 0.160 | 3 | 36993661 | missense variant | C/A;G;T | snv | 4.0E-06 | 1 | ||
| rs63750648 | 0.882 | 0.160 | 3 | 36993602 | missense variant | A/T | snv | 1 | |||
| rs63749994 | 1.000 | 0.080 | 3 | 36993638 | missense variant | GC/TG | mnv | 1 | |||
| rs63751012 | 0.851 | 0.200 | 3 | 36993656 | stop gained | G/A;C;T | snv | 1 | |||
| rs63750792 | 0.925 | 0.160 | 3 | 36993630 | missense variant | C/T | snv | 1 | |||
| rs28930073 | 0.827 | 0.200 | 3 | 37007004 | missense variant | G/C | snv | 2.1E-04 | 1.9E-04 | 1 | |
| rs267607894 | 0.925 | 0.160 | 3 | 37050628 | missense variant | T/A;C | snv | 1 | |||
| rs63750268 | 1.000 | 0.080 | 3 | 37020399 | missense variant | G/A | snv | 4.4E-05 | 2.1E-05 | 1 | |
| rs63751267 | 1.000 | 0.080 | 3 | 36996663 | missense variant | G/A | snv | 1 | |||
| rs63750437 | 0.925 | 0.160 | 3 | 37000977 | missense variant | G/A;C | snv | 1 | |||
| rs63750718 | 1.000 | 0.080 | 3 | 37047589 | missense variant | A/G | snv | 1 | |||
| rs63750650 | 1.000 | 0.080 | 3 | 37017518 | missense variant | A/G | snv | 2.5E-04 | 1.3E-04 | 1 | |
| rs63751283 | 0.925 | 0.160 | 3 | 37014533 | missense variant | T/A;G | snv | 1 | |||
| rs63749939 | 0.851 | 0.160 | 3 | 36996702 | missense variant | G/A | snv | 1 | |||
| rs63750498 | 1.000 | 0.080 | 3 | 37028789 | missense variant | G/A;T | snv | 2.4E-05 | 1 | ||
| rs63749803 | 1.000 | 0.080 | 3 | 37004421 | missense variant | T/C;G | snv | 1 | |||
| rs63750297 | 1.000 | 0.080 | 3 | 37004412 | missense variant | C/A;G;T | snv | 8.0E-06 | 1 | ||
| rs63751047 | 1.000 | 0.080 | 3 | 37048525 | missense variant | C/A;G | snv | 1 | |||
| rs587779005 | 1.000 | 0.080 | 3 | 37004425 | missense variant | G/C | snv | 1 |