| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1299491 | 19 | 49916142 | intron variant | A/C | snv | 0.70 | 1 | ||||
| rs370867162 | 10 | 52768257 | missense variant | G/A;T | snv | 6.4E-05 | 8.4E-05 | 1 | |||
| rs4976846 | 13 | 109168863 | intron variant | T/C | snv | 0.29 | 1 | ||||
| rs4972431 | 2 | 174134460 | intron variant | C/T | snv | 0.53 | 1 | ||||
| rs10838427 | 11 | 45160131 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs780935825 | 9 | 117713547 | synonymous variant | C/T | snv | 1.2E-05 | 1 | ||||
| rs2406176 | 21 | 18347109 | intron variant | T/G | snv | 0.72 | 1 |