| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11571111 | 1 | 204161105 | intron variant | C/A | snv | 5.0E-03 | 4 | ||||
| rs12748152 | 1.000 | 0.120 | 1 | 26811902 | upstream gene variant | C/T | snv | 5.7E-02 | 5 | ||
| rs1456649 | 1 | 240288305 | intron variant | G/C | snv | 3.0E-03 | 5 | ||||
| rs17315646 | 1 | 230159560 | intron variant | C/A;G | snv | 0.45 | 3 | ||||
| rs2144300 | 0.882 | 0.040 | 1 | 230159169 | intron variant | C/T | snv | 0.44 | 4 | ||
| rs2281719 | 1.000 | 0.040 | 1 | 230161913 | intron variant | C/T | snv | 0.45 | 3 | ||
| rs2296065 | 1 | 230166030 | intron variant | G/A;C | snv | 3 | |||||
| rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
| rs3753600 | 1 | 53125615 | intron variant | G/A | snv | 3.0E-03 | 3 | ||||
| rs480392 | 1 | 107436774 | synonymous variant | A/C | snv | 0.99 | 0.95 | 3 | |||
| rs4846914 | 0.925 | 0.080 | 1 | 230159944 | intron variant | G/A | snv | 0.45 | 4 | ||
| rs4846918 | 1 | 230164840 | intron variant | C/G;T | snv | 3 | |||||
| rs4970834 | 0.925 | 0.160 | 1 | 109272258 | intron variant | C/T | snv | 0.17 | 0.21 | 6 | |
| rs5176 | 1 | 53246137 | 3 prime UTR variant | T/G | snv | 6.4E-04 | 6 | ||||
| rs611841 | 1 | 230173735 | intron variant | C/A;G | snv | 3 | |||||
| rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 8 | ||
| rs6668858 | 1 | 204166660 | intron variant | G/A | snv | 9.7E-03 | 4 | ||||
| rs1000879 | 2 | 218439407 | intron variant | G/A | snv | 4.1E-02 | 3 | ||||
| rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 7 | |
| rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 | ||||
| rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
| rs13389219 | 1.000 | 0.080 | 2 | 164672366 | intron variant | C/T | snv | 0.47 | 5 | ||
| rs2678379 | 1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 | 7 | ||
| rs2972146 | 0.882 | 0.040 | 2 | 226235982 | intergenic variant | G/T | snv | 0.72 | 3 | ||
| rs34183407 | 2 | 73454052 | missense variant | C/T | snv | 2.1E-05 | 3.5E-05 | 6 |