| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72549325 | 1.000 | 0.080 | 1 | 171107795 | stop gained | G/A;T | snv | 2.0E-05; 4.0E-06 | 2 | ||
| rs1384237868 | 1.000 | 0.080 | 1 | 171107723 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs28363549 | 1.000 | 0.080 | 1 | 171108207 | missense variant | C/T | snv | 2.0E-04 | 3.5E-05 | 1 | |
| rs3832024 | 1.000 | 0.080 | 1 | 171108183 | stop gained | TG/- | delins | 1 | |||
| rs572292275 | 1.000 | 0.080 | 1 | 171114108 | missense variant | C/T | snv | 1.2E-04 | 6.3E-05 | 1 | |
| rs61753344 | 1.000 | 0.080 | 1 | 171114092 | stop gained | G/A;T | snv | 2.9E-04 | 1 | ||
| rs72549320 | 1.000 | 0.080 | 1 | 171092752 | missense variant | G/A | snv | 1 | |||
| rs72549322 | 1.000 | 0.080 | 1 | 171103834 | missense variant | A/G | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs72549323 | 1.000 | 0.080 | 1 | 171103850 | missense variant | G/C;T | snv | 8.0E-06 | 1 | ||
| rs72549326 | 1.000 | 0.080 | 1 | 171107811 | missense variant | C/T | snv | 1.0E-03 | 1.5E-03 | 1 | |
| rs72549330 | 1.000 | 0.080 | 1 | 171114119 | stop gained | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs72549331 | 1.000 | 0.080 | 1 | 171114339 | missense variant | G/A;T | snv | 1.1E-04 | 1 | ||
| rs72549332 | 1.000 | 0.080 | 1 | 171117145 | missense variant | G/A | snv | 5.6E-05 | 7.0E-05 | 1 | |
| rs72549333 | 1.000 | 0.080 | 1 | 171117267 | missense variant | G/A | snv | 5.6E-05 | 4.2E-05 | 1 | |
| rs72549334 | 1.000 | 0.080 | 1 | 171117317 | missense variant | C/T | snv | 1.2E-04 | 1.8E-04 | 1 | |
| rs748324481 | 1.000 | 0.080 | 1 | 171110883 | missense variant | G/A;C;T | snv | 2.4E-05; 8.0E-06; 8.0E-06 | 1 | ||
| rs72549321 | 1.000 | 0.080 | 1 | 171103806 | missense variant | G/A | snv | 4.0E-06 | 1 |