| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 12 | ||
| rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 8 | ||
| rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 4 | ||
| rs77768175 | 1.000 | 0.040 | 12 | 112298314 | intron variant | A/G | snv | 5.8E-03 | 1 | ||
| rs2285809 | 1.000 | 0.120 | 12 | 112270622 | intron variant | T/C | snv | 0.16 | 1 |