| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
| rs7529925 | 1 | 199038079 | intron variant | C/T | snv | 0.77 | 4 | ||||
| rs1036332 | 1 | 199043349 | intron variant | A/C | snv | 0.70 | 3 | ||||
| rs322931 | 1.000 | 0.080 | 1 | 199050726 | intron variant | G/A | snv | 0.22 | 2 | ||
| rs115858175 | 1.000 | 0.040 | 1 | 199032122 | intron variant | C/A;G | snv | 1 | |||
| rs12125200 | 1 | 199022914 | intron variant | A/G | snv | 0.77 | 1 | ||||
| rs2360962 | 1 | 199035580 | intron variant | A/T | snv | 0.76 | 1 | ||||
| rs6427756 | 1 | 199031598 | intron variant | A/G | snv | 0.71 | 1 | ||||
| rs781255974 | 1 | 199025568 | intron variant | AAA/-;A;AA;AAAA;AAAAA | delins | 1 |