| 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 | |||
| rs121913503 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 23 | |||
| rs1057519736 | 0.752 | 0.160 | 15 | 90088605 | missense variant | C/G | snv | 13 | |||
| rs1353428252 | 0.851 | 0.120 | 15 | 90088681 | missense variant | A/C | snv | 8.0E-06 | 5 | ||
| rs1162844242 | 0.925 | 0.120 | 3 | 38138711 | missense variant | G/T | snv | 7.0E-06 | 2 | ||
| rs747931353 | 1.000 | 0.080 | 1 | 207454468 | missense variant | G/A;T | snv | 5.1E-06; 5.1E-06 | 1 | ||
| rs1413407735 | 1.000 | 0.080 | 3 | 49360964 | missense variant | T/G | snv | 7.0E-06 | 1 |