| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894655 | 0.925 | 0.120 | 17 | 39665762 | stop gained | C/T | snv | 1.4E-05 | 3 | ||
| rs397516863 | 0.925 | 0.080 | 17 | 39666077 | missense variant | C/A;G;T | snv | 2 | |||
| rs1555606959 | 1.000 | 0.120 | 17 | 39665391 | frameshift variant | -/G | delins | 2 | |||
| rs778568339 | 0.925 | 0.080 | 17 | 39665382 | frameshift variant | -/AGGTGTCG | delins | 9.2E-05 | 1.4E-05 | 2 | |
| rs149585781 | 0.925 | 0.040 | 17 | 39666063 | missense variant | G/A | snv | 2.1E-04 | 2.1E-04 | 1 | |
| rs1555606976 | 17 | 39665448 | frameshift variant | GT/- | delins | 1 | |||||
| rs1567864804 | 1.000 | 0.080 | 17 | 39665360 | start lost | A/G | snv | 1 | |||
| rs45495192 | 1.000 | 0.120 | 17 | 39665391 | stop gained | C/A;G;T | snv | 4.0E-06; 2.7E-04; 1.0E-03 | 1 | ||
| rs786205076 | 1.000 | 0.120 | 17 | 39665467 | splice donor variant | GG/- | delins | 1 | |||
| rs863224933 | 1.000 | 0.120 | 17 | 39665383 | stop gained | -/GAGGTGT | delins | 1 | |||
| rs773317399 | 1.000 | 17 | 39666015 | missense variant | C/A;T | snv | 1.6E-05 | 1 |