| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34782622 | 7 | 2155497 | intron variant | A/G | snv | 0.14 | 1 | ||||
| rs62442924 | 7 | 1950341 | intron variant | C/T | snv | 0.17 | 1 | ||||
| rs71525361 | 7 | 2120142 | intron variant | T/A;C | snv | 1 | |||||
| rs527510716 | 1.000 | 0.080 | 7 | 1904901 | intron variant | G/C | snv | 0.14 | 1 | ||
| rs3800917 | 1.000 | 7 | 2128304 | intron variant | G/A | snv | 0.28 | 1 | |||
| rs3996330 | 7 | 1979188 | intron variant | C/A | snv | 0.54 | 1 | ||||
| rs56072378 | 1.000 | 0.040 | 7 | 2064729 | intron variant | A/G | snv | 0.29 | 1 | ||
| rs2056477 | 1.000 | 0.040 | 7 | 2040109 | intron variant | G/A;C;T | snv | 1 | |||
| rs4721089 | 7 | 1833285 | intron variant | C/T | snv | 0.80 | 1 | ||||
| rs1860826 | 7 | 2072871 | intron variant | G/A;T | snv | 1 | |||||
| rs10267593 | 1.000 | 0.040 | 7 | 1897625 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs11772232 | 7 | 1816637 | intron variant | C/T | snv | 0.13 | 1 | ||||
| rs6963853 | 7 | 1819089 | intron variant | G/A | snv | 0.48 | 1 |