| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1805032 | 1.000 | 0.040 | 2 | 151839238 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
| rs74315322 | 1.000 | 0.040 | 1 | 154275165 | stop gained | C/T | snv | 3.6E-05 | 3 | ||
| rs121918413 | 1.000 | 0.120 | 5 | 151851470 | missense variant | G/T | snv | 3 | |||
| rs80358261 | 0.925 | 0.160 | 14 | 74486404 | missense variant | C/T | snv | 1.7E-05 | 1.4E-05 | 3 | |
| rs121913223 | 1.000 | 0.040 | 5 | 80633904 | missense variant | T/A | snv | 4.0E-06 | 2 | ||
| rs1467252662 | 5 | 151851530 | missense variant | G/T | snv | 4.0E-06 | 2 | ||||
| rs1280914556 | 1 | 32014269 | missense variant | A/G | snv | 2.1E-05 | 2 | ||||
| rs771884087 | 1.000 | 0.080 | 20 | 45253726 | synonymous variant | T/C | snv | 2 | |||
| rs756915170 | 19 | 49909654 | missense variant | T/C | snv | 4.0E-06 | 2 | ||||
| rs749191312 | 1.000 | 0.080 | 20 | 18497075 | synonymous variant | C/T | snv | 4.0E-06 | 2 | ||
| rs374651285 | 4 | 73406645 | missense variant | G/A | snv | 1 | |||||
| rs13963 | 3 | 45035631 | missense variant | G/A | snv | 0.49 | 0.43 | 1 | |||
| rs1457713736 | 8 | 11850867 | stop gained | C/T | snv | 7.0E-06 | 1 | ||||
| rs1471980111 | 6 | 38737948 | missense variant | G/A | snv | 4.1E-06 | 7.0E-06 | 1 |