| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs114930262 | 1.000 | 16 | 31459990 | missense variant | C/G;T | snv | 1.7E-05; 1.6E-03 | 1 | |||
| rs1293014259 | 1.000 | 16 | 31462499 | missense variant | C/G;T | snv | 8.1E-06 | 1 | |||
| rs1385397608 | 1.000 | 16 | 31462631 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
| rs1415974570 | 1.000 | 16 | 31462491 | missense variant | G/A | snv | 4.0E-06 | 1 | |||
| rs200951744 | 1.000 | 16 | 31466273 | missense variant | C/G | snv | 1.7E-03 | 1.7E-03 | 1 | ||
| rs35461188 | 1.000 | 16 | 31462515 | missense variant | G/C | snv | 1.1E-03 | 6.6E-04 | 1 | ||
| rs369721476 | 1.000 | 16 | 31462346 | stop gained | C/T | snv | 4.1E-06 | 7.0E-06 | 1 | ||
| rs370836071 | 1.000 | 16 | 31465913 | missense variant | C/T | snv | 6.1E-05 | 5.6E-05 | 1 | ||
| rs587777659 | 1.000 | 16 | 31466773 | missense variant | C/T | snv | 1 | ||||
| rs587777660 | 1.000 | 16 | 31459780 | stop gained | C/T | snv | 1 | ||||
| rs587777661 | 1.000 | 16 | 31464666 | missense variant | T/C | snv | 1 | ||||
| rs587777662 | 1.000 | 16 | 31464800 | missense variant | C/T | snv | 4.4E-06 | 2.1E-05 | 1 | ||
| rs587777663 | 1.000 | 16 | 31462641 | missense variant | T/C | snv | 1 |