| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 63 | |||
| rs1225976306 | 0.807 | 0.160 | 7 | 140924673 | missense variant | C/T | snv | 9.3E-06 | 8 | ||
| rs398122527 | 0.882 | 0.080 | 7 | 97021048 | missense variant | C/A | snv | 3 | |||
| rs863225437 | 0.882 | 0.080 | 2 | 173232359 | missense variant | T/G | snv | 3 | |||
| rs761885185 | 0.882 | 0.120 | 3 | 189869329 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs587777842 | 1.000 | 0.080 | 7 | 97024509 | stop gained | C/A | snv | 1 |