Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
| rs121918598 | 0.851 | 0.080 | 1 | 237648523 | missense variant | G/A;C | snv | 4 | |||
| rs190140598 | 0.851 | 0.120 | 1 | 237445488 | missense variant | C/A;T | snv | 1.2E-05 | 4 | ||
| rs121918600 | 0.882 | 0.080 | 1 | 237791441 | missense variant | C/T | snv | 5 | |||
| rs121918603 | 0.882 | 0.080 | 1 | 237639068 | missense variant | C/T | snv | 3 | |||
| rs121918604 | 0.882 | 0.080 | 1 | 237798037 | missense variant | G/A;T | snv | 1.7E-05 | 3 | ||
| rs1273246817 | 0.882 | 0.080 | 1 | 237784169 | missense variant | A/C | snv | 3 | |||
| rs121918602 | 0.925 | 0.120 | 1 | 237454396 | missense variant | T/C | snv | 3 | |||
| rs121918606 | 0.925 | 0.080 | 1 | 237819181 | missense variant | C/G | snv | 3 | |||
| rs1458500258 | 0.925 | 0.080 | 1 | 237388098 | missense variant | G/T | snv | 7.0E-06 | 3 | ||
| rs794728721 | 0.925 | 0.080 | 1 | 237445489 | missense variant | G/A | snv | 3 | |||
| rs121918597 | 0.925 | 0.080 | 1 | 237634937 | missense variant | C/T | snv | 2 | |||
| rs121918599 | 0.925 | 0.080 | 1 | 237784024 | missense variant | C/G | snv | 2 | |||
| rs121918601 | 0.925 | 0.120 | 1 | 237640938 | missense variant | A/T | snv | 2 | |||
| rs121918605 | 0.925 | 0.080 | 1 | 237784314 | missense variant | A/G | snv | 2 | |||
| rs730880199 | 0.925 | 0.080 | 1 | 237819167 | missense variant | T/G | snv | 2 | |||
| rs764772142 | 0.925 | 0.080 | 1 | 237377349 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
| rs769219555 | 0.925 | 0.120 | 1 | 237648612 | missense variant | C/T | snv | 4.2E-05 | 8.4E-05 | 2 | |
| rs794728811 | 0.925 | 0.080 | 1 | 237832619 | missense variant | G/A | snv | 2 | |||
| rs1401116572 | 1.000 | 0.080 | 1 | 237441382 | missense variant | G/A | snv | 2 | |||
| rs1415931588 | 1.000 | 0.080 | 1 | 237377426 | missense variant | A/T | snv | 2 | |||
| rs1060500137 | 1.000 | 0.080 | 1 | 237772077 | missense variant | G/A | snv | 1 | |||
| rs1060500142 | 1.000 | 0.080 | 1 | 237330939 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1185619003 | 1.000 | 0.080 | 1 | 237830557 | missense variant | A/G | snv | 1 | |||
| rs1188352725 | 1.000 | 0.080 | 1 | 237798091 | missense variant | G/C | snv | 1 |