| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs2477686 | 0.807 | 0.040 | 1 | 2461209 | intron variant | G/C | snv | 0.64 | 7 | ||
| rs10842262 | 0.851 | 0.040 | 12 | 24031610 | intron variant | G/C | snv | 0.43 | 5 | ||
| rs6080550 | 0.851 | 0.040 | 20 | 1778944 | intron variant | C/G;T | snv | 9.6E-02 | 5 | ||
| rs12097821 | 0.882 | 0.040 | 1 | 106793679 | regulatory region variant | G/A;T | snv | 4 |