| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913135 | 0.882 | 0.120 | 19 | 7125437 | missense variant | C/A | snv | 3 | |||
| rs121913139 | 1.000 | 0.120 | 19 | 7122662 | missense variant | C/T | snv | 2 | |||
| rs121913142 | 0.925 | 0.120 | 19 | 7172333 | missense variant | A/C | snv | 2 | |||
| rs121913144 | 0.925 | 0.200 | 19 | 7125462 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs121913147 | 0.925 | 0.120 | 19 | 7170554 | missense variant | T/C | snv | 7.0E-06 | 2 | ||
| rs121913156 | 0.925 | 0.120 | 19 | 7120677 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs1329693158 | 0.925 | 0.120 | 19 | 7184454 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs1135401741 | 1.000 | 0.120 | 19 | 7125381 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1135401742 | 1.000 | 0.120 | 19 | 7170555 | missense variant | T/C | snv | 1 | |||
| rs121913138 | 1.000 | 0.120 | 19 | 7143072 | missense variant | C/A | snv | 1 | |||
| rs121913140 | 1.000 | 0.120 | 19 | 7119563 | stop gained | C/G;T | snv | 1 | |||
| rs121913146 | 1.000 | 0.120 | 19 | 7267518 | stop gained | C/T | snv | 1 | |||
| rs121913148 | 1.000 | 0.120 | 19 | 7125482 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs121913154 | 1.000 | 0.120 | 19 | 7122658 | missense variant | G/A;T | snv | 1 | |||
| rs1295645322 | 1.000 | 0.120 | 19 | 7120665 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs52800171 | 1.000 | 0.120 | 19 | 7120620 | missense variant | C/A | snv | 1 | |||
| rs52826008 | 1.000 | 0.120 | 19 | 7117072 | missense variant | C/G;T | snv | 1.2E-05; 3.5E-04 | 1 | ||
| rs938519025 | 1.000 | 0.120 | 19 | 7267498 | missense variant | C/A;T | snv | 1 |