| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909641 | 0.763 | 0.520 | 8 | 38419720 | missense variant | G/A | snv | 9 | |||
| rs515726224 | 0.925 | 0.320 | 8 | 38417962 | missense variant | C/T | snv | 3 | |||
| rs1563436265 | 1.000 | 0.280 | 8 | 38414875 | missense variant | C/G | snv | 2 | |||
| rs1554548253 | 1.000 | 0.280 | 8 | 38414835 | missense variant | C/T | snv | 1 | |||
| rs1554551657 | 1.000 | 0.280 | 8 | 38417363 | inframe deletion | ATC/- | delins | 1 | |||
| rs1554551667 | 1.000 | 0.280 | 8 | 38417365 | missense variant | A/T | snv | 1 | |||
| rs1563433902 | 1.000 | 0.280 | 8 | 38414611 | missense variant | A/G | snv | 1 | |||
| rs397515481 | 1.000 | 0.280 | 8 | 38428048 | missense variant | A/G | snv | 1 | |||
| rs398122945 | 1.000 | 0.280 | 8 | 38414164 | missense variant | C/T | snv | 1 | |||
| rs398122946 | 1.000 | 0.280 | 8 | 38414889 | missense variant | C/A | snv | 1 | |||
| rs780009859 | 1.000 | 0.280 | 8 | 38414887 | missense variant | G/A;C | snv | 3.2E-05 | 1.4E-05 | 1 | |
| rs869025669 | 1.000 | 0.280 | 8 | 38427970 | missense variant | A/G | snv | 1 | |||
| rs869025670 | 1.000 | 0.280 | 8 | 38417954 | missense variant | C/G;T | snv | 1 | |||
| rs869025671 | 1.000 | 0.280 | 8 | 38414876 | missense variant | C/G | snv | 1 | |||
| rs869025672 | 0.925 | 0.320 | 8 | 38414872 | missense variant | A/C;G | snv | 8.0E-06 | 1 | ||
| rs876661332 | 1.000 | 0.280 | 8 | 38417968 | missense variant | C/A | snv | 1 |