| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893915 | 0.776 | 0.200 | 5 | 149980428 | missense variant | C/T | snv | 9.8E-04 | 1.0E-03 | 10 | |
| rs1057518908 | 0.882 | 0.120 | 12 | 47984112 | missense variant | C/T | snv | 6 | |||
| rs766335907 | 0.851 | 0.200 | 19 | 18787632 | missense variant | G/A;T | snv | 8.0E-06; 8.0E-06 | 4 | ||
| rs28936368 | 0.882 | 0.080 | 19 | 18783129 | missense variant | G/A;T | snv | 8.6E-04 | 3 | ||
| rs781754383 | 0.882 | 0.080 | 4 | 109960942 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs104893645 | 0.925 | 0.080 | 2 | 20005953 | missense variant | A/T | snv | 2 | |||
| rs3776070 | 1.000 | 0.080 | 5 | 149981658 | missense variant | A/G;T | snv | 4.0E-05; 0.17 | 1 |