| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs35996865 | 0.851 | 0.280 | 18 | 21112383 | upstream gene variant | T/G | snv | 0.28 | 4 | ||
| rs1481280 | 1.000 | 0.080 | 18 | 21075490 | intron variant | C/A | snv | 0.31 | 2 | ||
| rs112108028 | 1.000 | 0.200 | 18 | 20959861 | missense variant | G/A | snv | 1 | |||
| rs111874856 | 1.000 | 0.200 | 18 | 21028924 | missense variant | C/T | snv | 1 | |||
| rs112130712 | 1.000 | 0.200 | 18 | 20967783 | missense variant | T/C | snv | 1 | |||
| rs73963110 | 1.000 | 0.080 | 18 | 21098353 | intron variant | T/C;G | snv | 1 | |||
| rs531292167 | 1.000 | 0.080 | 18 | 21006431 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
| rs2271255 | 1.000 | 0.080 | 18 | 21044113 | missense variant | T/C | snv | 3.6E-05 | 7.0E-06 | 1 | |
| rs288979 | 1.000 | 0.080 | 18 | 21031282 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs56085230 | 1.000 | 0.080 | 18 | 21042578 | synonymous variant | G/A | snv | 6.7E-03 | 6.3E-03 | 1 | |
| rs288980 | 1.000 | 0.080 | 18 | 21029619 | intron variant | T/C | snv | 0.66 | 1 | ||
| rs7237677 | 1.000 | 0.080 | 18 | 20979714 | intron variant | G/C | snv | 0.53 | 1 |