| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 58 | |
| rs758272654 | 0.611 | 0.680 | 20 | 58909201 | synonymous variant | T/C | snv | 4.0E-06 | 7.0E-06 | 50 | |
| rs9904341 | 0.695 | 0.280 | 17 | 78214286 | 5 prime UTR variant | G/A;C;T | snv | 0.38; 4.8E-06 | 20 | ||
| rs2011077 | 0.807 | 0.080 | 5 | 177094455 | intron variant | C/T | snv | 0.19 | 8 | ||
| rs776973438 | 1.000 | 19 | 50860060 | missense variant | C/T | snv | 4.0E-06 | 1 | |||
| rs1713418 | 1.000 | 14 | 20366650 | 3 prime UTR variant | A/G | snv | 0.52 | 1 | |||
| rs1760904 | 1.000 | 14 | 20383870 | missense variant | A/C;G | snv | 8.5E-06; 4.2E-06; 0.56 | 0.62 | 1 |