| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs749714198 | 0.882 | 0.200 | 9 | 21971100 | missense variant | G/A | snv | 8.6E-06 | 7.0E-06 | 1 | |
| rs1554653960 | 0.925 | 0.040 | 9 | 21971007 | missense variant | C/T | snv | 1 | |||
| rs876658534 | 0.925 | 0.120 | 9 | 21971156 | missense variant | GC/AA | mnv | 1 | |||
| rs878853647 | 0.882 | 0.120 | 9 | 21971099 | missense variant | C/G;T | snv | 1 | |||
| rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 1 | ||
| rs137854597 | 1.000 | 9 | 21971094 | missense variant | C/T | snv | 4.3E-06 | 1 | |||
| rs137854599 | 0.882 | 0.080 | 9 | 21971093 | missense variant | C/G;T | snv | 1 | |||
| rs1057519883 | 0.742 | 0.280 | 9 | 21971120 | missense variant | C/G;T | snv | 1 |