| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893836 | 0.790 | 0.160 | 4 | 67754019 | missense variant | T/C | snv | 2.8E-03 | 2.3E-03 | 7 | |
| rs104894703 | 0.882 | 0.040 | 19 | 918604 | missense variant | T/C | snv | 2.5E-05 | 1.4E-05 | 3 | |
| rs104893842 | 0.925 | 0.040 | 4 | 67753920 | missense variant | C/T | snv | 1.4E-04 | 2.1E-04 | 2 | |
| rs104893843 | 0.925 | 0.040 | 4 | 67754306 | missense variant | A/T | snv | 1.3E-04 | 6.3E-05 | 2 | |
| rs1281091213 | 1.000 | 0.040 | 8 | 26864578 | missense variant | G/A;T | snv | 1 | |||
| rs748209924 | 1.000 | 0.040 | 6 | 32974462 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs515726223 | 1.000 | 0.040 | 8 | 38424655 | missense variant | T/G | snv | 1 | |||
| rs757813231 | 1.000 | 0.040 | 19 | 19626983 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 1 |