| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387907136 | 0.882 | 0.080 | 8 | 95247712 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 3 | |
| rs387907137 | 0.882 | 0.080 | 8 | 95247696 | missense variant | T/C | snv | 2 | |||
| rs1085307121 | 1.000 | 8 | 95269033 | splice donor variant | A/G | snv | 1 | ||||
| rs1064792853 | 1.000 | 8 | 95263776 | splice acceptor variant | T/C | snv | 1 | ||||
| rs748014296 | 1.000 | 8 | 95247686 | stop gained | C/T | snv | 8.0E-06 | 1 | |||
| rs1064792852 | 1.000 | 8 | 95247744 | stop gained | A/C;T | snv | 4.0E-06; 8.0E-06 | 1 | |||
| rs1060505042 | 1.000 | 8 | 95260534 | splice acceptor variant | T/G | snv | 7.0E-06 | 1 | |||
| rs766087213 | 1.000 | 8 | 95260472 | stop gained | T/A | snv | 8.8E-06 | 1 |