| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs772388824 | 1.000 | 0.080 | 4 | 174976138 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs544557652 | 1.000 | 0.080 | 4 | 174975617 | missense variant | C/T | snv | 1.0E-04 | 9.1E-05 | 1 | |
| rs267600087 | 1.000 | 0.080 | 4 | 174975856 | missense variant | G/A | snv | 1 | |||
| rs267600090 | 1.000 | 0.080 | 4 | 174976558 | missense variant | G/A | snv | 1 | |||
| rs866380131 | 1.000 | 0.080 | 4 | 174976226 | missense variant | C/T | snv | 1 | |||
| rs267600091 | 1.000 | 0.080 | 4 | 174976826 | missense variant | G/A | snv | 1 | |||
| rs140083180 | 1.000 | 0.080 | 4 | 174976294 | missense variant | A/T | snv | 1 | |||
| rs899870236 | 1.000 | 0.080 | 4 | 174976051 | missense variant | G/A | snv | 1 | |||
| rs267600093 | 1.000 | 0.080 | 4 | 174977122 | missense variant | C/T | snv | 1 | |||
| rs267600089 | 1.000 | 0.080 | 4 | 174976439 | missense variant | G/A | snv | 4.2E-06 | 1 | ||
| rs150047888 | 1.000 | 0.080 | 4 | 174976733 | missense variant | G/A | snv | 8.0E-06 | 1 |