| 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 | |||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 144 | ||
| rs121913500 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 96 | ||
| rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 57 | ||
| rs1034749666 | 0.776 | 0.160 | 21 | 33027257 | missense variant | G/A | snv | 9 | |||
| rs199643834 | 0.827 | 0.200 | 17 | 17215000 | missense variant | T/C | snv | 1.9E-04 | 1.7E-04 | 6 | |
| rs764882391 | 1.000 | 0.040 | 1 | 155187358 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
| rs772667594 | 1.000 | 0.040 | 1 | 155187332 | missense variant | T/C | snv | 8.0E-06 | 1 |