| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607261 | 0.807 | 0.280 | 2 | 27312753 | stop gained | C/T | snv | 8.0E-06 | 28 | ||
| rs368900406 | 0.827 | 0.160 | 2 | 27312255 | non coding transcript exon variant | A/C | snv | 8.0E-06 | 2.1E-05 | 27 | |
| rs781565158 | 0.851 | 0.120 | 12 | 21452130 | missense variant | A/G | snv | 4.7E-05 | 2.1E-05 | 22 | |
| rs1563452941 | 0.882 | 0.120 | 8 | 42437137 | stop gained | C/A | snv | 13 | |||
| rs80356702 | 0.882 | 0.120 | 7 | 143330868 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 9 | |
| rs28933383 | 0.851 | 0.120 | 12 | 4912055 | missense variant | C/A;G;T | snv | 8 | |||
| rs1057518962 | X | 32573812 | stop gained | C/A;G;T | snv | 5.5E-06; 5.5E-06 | 6 | ||||
| rs202085145 | 1.000 | 0.080 | 12 | 56002720 | missense variant | G/T | snv | 1.0E-03 | 5.6E-04 | 6 | |
| rs114368325 | 0.925 | 0.120 | 20 | 54158136 | missense variant | G/A;C | snv | 6.6E-04; 8.0E-06 | 4 |