| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555438212 | 1.000 | 0.120 | 15 | 68208239 | stop gained | C/T | snv | 1 | |||
| rs1555438411 | 1.000 | 0.120 | 15 | 68209637 | stop gained | C/T | snv | 1 | |||
| rs1555438443 | 1.000 | 0.120 | 15 | 68209759 | stop gained | C/T | snv | 1 | |||
| rs746753722 | 1.000 | 0.120 | 15 | 68208397 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs763944821 | 1.000 | 0.120 | 15 | 68229536 | missense variant | C/T | snv | 8.2E-04 | 9.8E-05 | 1 | |
| rs154774639 | 1.000 | 0.120 | 15 | 68208186 | frameshift variant | G/- | delins | 1.4E-05 | 1 | ||
| rs587779408 | 0.882 | 0.160 | 11 | 6391804 | missense variant | G/A | snv | 2.4E-05 | 2.8E-05 | 3 | |
| rs758921701 | 1.000 | 0.120 | 15 | 68208180 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs919850756 | 1.000 | 0.120 | 15 | 68211685 | missense variant | G/A | snv | 1 | |||
| rs104894486 | 1.000 | 0.120 | 15 | 68209639 | stop gained | G/A;C | snv | 1 | |||
| rs747229909 | 1.000 | 0.120 | 15 | 68211716 | missense variant | G/A;C | snv | 5.6E-05 | 1 | ||
| rs154774640 | 0.925 | 0.120 | 15 | 68218584 | stop gained | G/C | snv | 8.0E-06 | 2.1E-05 | 2 | |
| rs1194940137 | 1.000 | 0.120 | 15 | 68208187 | missense variant | G/T | snv | 4.0E-06 | 1 | ||
| rs768422260 | 0.925 | 0.120 | 15 | 68208280 | inframe deletion | GAG/- | delins | 1.4E-05 | 2 | ||
| rs1555440206 | 1.000 | 0.120 | 15 | 68229584 | start lost | T/C | snv | 1 | |||
| rs764571295 | 1.000 | 0.120 | 15 | 68209640 | missense variant | T/C;G | snv | 1.6E-05; 2.4E-05 | 1 | ||
| rs1555438234 | 1.000 | 0.120 | 15 | 68208306 | frameshift variant | TGTCC/- | delins | 1 |