| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12913832 | 0.763 | 0.200 | 15 | 28120472 | intron variant | A/G | snv | 0.50 | 15 | ||
| rs1667394 | 15 | 28285036 | intron variant | C/A;T | snv | 5 | |||||
| rs916977 | 1.000 | 0.080 | 15 | 28268218 | intron variant | T/C;G | snv | 5 | |||
| rs121918166 | 0.925 | 0.160 | 15 | 27985101 | missense variant | C/T | snv | 3.0E-03 | 3.4E-03 | 5 | |
| rs141949212 | 0.882 | 0.160 | 15 | 27845052 | missense variant | C/T | snv | 4.0E-05 | 2.0E-04 | 5 | |
| rs121918167 | 0.925 | 0.160 | 15 | 27871170 | missense variant | G/A | snv | 1.1E-04 | 2.2E-04 | 4 | |
| rs121918170 | 1.000 | 0.160 | 15 | 27983383 | missense variant | T/A;C | snv | 3.5E-04 | 4.2E-04 | 3 | |
| rs368124046 | 1.000 | 0.160 | 15 | 27983340 | splice region variant | C/T | snv | 4.0E-06 | 7.7E-05 | 2 | |
| rs776814755 | 1.000 | 0.160 | 15 | 27851390 | missense variant | C/T | snv | 3.2E-05 | 7.0E-06 | 2 |