| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6689858 | 0.724 | 0.240 | 1 | 197406337 | intron variant | T/C | snv | 0.39 | 14 | ||
| rs76169311 | 1.000 | 0.120 | 1 | 197372771 | intron variant | G/A | snv | 0.13 | 2 | ||
| rs2759663 | 0.925 | 0.080 | 1 | 197415296 | intron variant | C/G;T | snv | 2 | |||
| rs2786098 | 1.000 | 0.080 | 1 | 197356778 | intron variant | T/A;G | snv | 1 | |||
| rs2786107 | 1 | 197341647 | intron variant | G/T | snv | 0.80 | 1 | ||||
| rs12042924 | 1 | 197328287 | intron variant | T/C | snv | 0.41 | 1 | ||||
| rs10754220 | 1 | 197275160 | intron variant | G/A | snv | 0.22 | 1 | ||||
| rs1009188 | 1 | 197287960 | intron variant | T/C | snv | 0.22 | 1 |