| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121908726 | 0.851 | 0.160 | 20 | 44626570 | missense variant | G/C;T | snv | 4.0E-06 | 4 | ||
| rs121908727 | 0.851 | 0.160 | 20 | 44624272 | missense variant | G/T | snv | 1.2E-05 | 4 | ||
| rs121908723 | 0.851 | 0.240 | 20 | 44623039 | missense variant | C/T | snv | 1.2E-05 | 5.6E-05 | 4 | |
| rs121908735 | 0.882 | 0.160 | 20 | 44625581 | missense variant | G/A | snv | 1.4E-05 | 3 | ||
| rs121908715 | 0.882 | 0.240 | 20 | 44620391 | missense variant | G/A | snv | 5.2E-05 | 2.0E-04 | 3 | |
| rs121908721 | 0.882 | 0.160 | 20 | 44621121 | missense variant | G/A;C | snv | 2.4E-05 | 3 | ||
| rs121908740 | 0.882 | 0.160 | 20 | 44623054 | missense variant | G/A | snv | 1.3E-04 | 7.0E-06 | 3 | |
| rs121908714 | 0.925 | 0.160 | 20 | 44626516 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs121908722 | 0.925 | 0.160 | 20 | 44625580 | missense variant | C/A;G;T | snv | 2 | |||
| rs121908724 | 0.925 | 0.160 | 20 | 44636264 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
| rs121908739 | 0.925 | 0.160 | 20 | 44626498 | missense variant | A/G | snv | 7.2E-05 | 7.0E-05 | 2 | |
| rs1555844617 | 0.925 | 0.120 | 20 | 44625650 | frameshift variant | -/T | delins | 2 | |||
| rs199422328 | 0.925 | 0.160 | 20 | 44626597 | missense variant | C/A | snv | 8.0E-06 | 8.4E-05 | 2 | |
| rs387906267 | 0.925 | 0.160 | 20 | 44626601 | splice acceptor variant | T/C | snv | 2 | |||
| rs761242509 | 0.925 | 0.160 | 20 | 44625568 | splice donor variant | C/T | snv | 2.1E-05 | 2.8E-05 | 2 | |
| rs780014431 | 0.925 | 0.120 | 20 | 44625623 | stop gained | G/A | snv | 2.0E-05 | 7.0E-06 | 2 | |
| rs121908716 | 0.925 | 0.160 | 20 | 44623053 | missense variant | C/T | snv | 7.2E-05 | 9.8E-05 | 2 | |
| rs121908718 | 0.925 | 0.160 | 20 | 44621103 | missense variant | G/A;T | snv | 8.0E-06; 2.8E-05 | 2 | ||
| rs1057520217 | 1.000 | 20 | 44651601 | stop gained | G/A | snv | 1 | ||||
| rs121908717 | 1.000 | 20 | 44626517 | missense variant | G/A | snv | 1.4E-05 | 1 | |||
| rs121908719 | 1.000 | 20 | 44624279 | missense variant | C/T | snv | 2.0E-05 | 1 | |||
| rs121908725 | 1.000 | 20 | 44636279 | missense variant | G/C | snv | 8.3E-06 | 1.4E-05 | 1 | ||
| rs121908730 | 1.000 | 20 | 44626598 | missense variant | C/A | snv | 1 | ||||
| rs121908731 | 1.000 | 20 | 44625662 | missense variant | C/A;T | snv | 1 | ||||
| rs121908732 | 1.000 | 20 | 44625628 | missense variant | C/G;T | snv | 5.0E-06 | 1 |