| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs779507031 | 1.000 | 0.080 | 6 | 18122408 | stop gained | C/A;G;T | snv | 1.0E-05 | 1 | ||
| rs1193718748 | 1.000 | 0.080 | 6 | 18122470 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs757759398 | 1.000 | 0.080 | 6 | 18122509 | missense variant | A/C;G | snv | 4.5E-06; 4.5E-06 | 1 | ||
| rs28940575 | 0.925 | 0.080 | 6 | 18122531 | missense variant | A/T | snv | 8.9E-06 | 7.0E-06 | 2 | |
| rs514492 | 0.882 | 0.160 | 9 | 35062975 | splice region variant | C/T | snv | 0.75 | 0.75 | 3 | |
| rs33949390 | 0.776 | 0.160 | 12 | 40320043 | missense variant | G/A;C;T | snv | 1.6E-04; 1.9E-03; 8.0E-06 | 9 | ||
| rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 |