| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs768407867 | 0.925 | 0.160 | 2 | 174748177 | missense variant | C/T | snv | 4.4E-05 | 3.5E-05 | 3 | |
| rs137852801 | 0.925 | 0.120 | 2 | 174754242 | missense variant | C/T | snv | 2 | |||
| rs121912670 | 0.925 | 0.120 | 2 | 232542992 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 2 | |
| rs267606726 | 0.925 | 0.120 | 2 | 232540681 | missense variant | T/G | snv | 2 | |||
| rs764266722 | 0.925 | 0.120 | 2 | 232540387 | stop gained | C/A;T | snv | 8.0E-06; 2.0E-05 | 2 | ||
| rs767503038 | 0.925 | 0.120 | 2 | 232543030 | frameshift variant | CT/- | del | 2.6E-04 | 2 | ||
| rs137852809 | 1.000 | 0.120 | 2 | 174753595 | missense variant | C/A;T | snv | 4.0E-06; 2.4E-05 | 1 | ||
| rs1060499782 | 1.000 | 0.120 | 2 | 232535130 | frameshift variant | GA/- | delins | 7.0E-06 | 1 | ||
| rs121909505 | 1.000 | 0.120 | 2 | 232527436 | stop gained | G/A;C | snv | 1.6E-05 | 1 | ||
| rs121909506 | 1.000 | 0.120 | 2 | 232528301 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs121909507 | 1.000 | 0.120 | 2 | 232535148 | stop gained | C/T | snv | 2.1E-05 | 1 | ||
| rs1553578312 | 1.000 | 0.120 | 2 | 232544541 | stop gained | C/T | snv | 1 | |||
| rs1490328834 | 1.000 | 0.120 | 3 | 81642817 | missense variant | T/C | snv | 4.0E-06 | 1 |