| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs76539814 | 0.925 | 0.120 | 1 | 155236384 | missense variant | G/A | snv | 1.2E-05 | 2 | ||
| rs121908305 | 1.000 | 0.120 | 1 | 155236379 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs121908306 | 1.000 | 0.120 | 1 | 155236328 | missense variant | A/C | snv | 1 | |||
| rs75636769 | 1.000 | 0.120 | 1 | 155238209 | missense variant | G/A;T | snv | 1.6E-05 | 1 | ||
| rs758447515 | 1.000 | 0.120 | 1 | 155239633 | stop gained | G/A;T | snv | 3.2E-05 | 1 | ||
| rs77284004 | 1.000 | 0.120 | 1 | 155235813 | missense variant | T/G | snv | 1 | |||
| rs77321207 | 1.000 | 0.120 | 1 | 155236441 | missense variant | T/C | snv | 1 | |||
| rs77738682 | 1.000 | 0.120 | 1 | 155235777 | missense variant | T/A;C | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs79696831 | 1.000 | 0.120 | 1 | 155237369 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 |