| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72549398 | 0.790 | 0.240 | 2 | 168932442 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 8 | |
| rs2109505 | 0.851 | 0.200 | 7 | 87450090 | splice region variant | T/A | snv | 0.21 | 0.22 | 6 | |
| rs375315619 | 0.851 | 0.080 | 7 | 87440230 | missense variant | T/C | snv | 2.0E-04 | 9.8E-05 | 4 | |
| rs111033609 | 0.882 | 0.200 | 18 | 57695188 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
| rs121909100 | 0.882 | 0.200 | 18 | 57669433 | missense variant | A/G | snv | 9.6E-05 | 9.1E-05 | 3 | |
| rs377160065 | 0.925 | 0.040 | 7 | 87453005 | stop gained | G/A | snv | 1.6E-05 | 1.4E-05 | 2 | |
| rs121909101 | 0.925 | 0.200 | 18 | 57674993 | missense variant | C/T | snv | 2 | |||
| rs121909098 | 0.925 | 0.040 | 18 | 57661207 | missense variant | C/T | snv | 2.0E-05 | 2.8E-05 | 2 | |
| rs1562945221 | 1.000 | 0.040 | 7 | 87402211 | frameshift variant | -/T | delins | 1 | |||
| rs1562976061 | 1.000 | 0.040 | 7 | 87440206 | frameshift variant | A/- | delins | 1 | |||
| rs121909099 | 1.000 | 0.040 | 18 | 57695248 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs121909104 | 1.000 | 0.040 | 18 | 57688361 | missense variant | G/A | snv | 1 | |||
| rs121909105 | 1.000 | 0.040 | 18 | 57674849 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs147642236 | 1.000 | 0.040 | 18 | 57684168 | missense variant | A/G;T | snv | 3.8E-04; 4.0E-06 | 1 | ||
| rs1438249656 | 1.000 | 0.040 | 18 | 57652627 | missense variant | C/T | snv | 1 | |||
| rs773092889 | 1.000 | 0.040 | 18 | 57661323 | missense variant | A/G | snv | 1.2E-05 | 1 | ||
| rs1337978497 | 1.000 | 0.040 | 18 | 57669352 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs1350369369 | 1.000 | 0.040 | 18 | 57668441 | missense variant | C/T | snv | 1 | |||
| rs387906381 | 1.000 | 0.040 | 18 | 57669316 | splice donor variant | A/G | snv | 1.3E-05 | 1 |