Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs149391489 | 1.000 | 0.160 | X | 101401803 | missense variant | T/C | snv | 3.3E-04 | 4.2E-04 | 1 | |
| rs148158093 | 0.925 | 0.200 | X | 101403828 | missense variant | G/A | snv | 2.2E-04 | 4.0E-04 | 3 | |
| rs111422676 | 1.000 | 0.160 | X | 101398011 | missense variant | C/T | snv | 5.5E-05 | 1.3E-04 | 1 | |
| rs727503950 | 1.000 | 0.160 | X | 101400712 | missense variant | A/G | snv | 1.1E-05 | 1.9E-05 | 1 | |
| rs869312304 | 1.000 | 0.160 | X | 101407860 | missense variant | G/A;T | snv | 1.9E-05 | 1 | ||
| rs104894833 | 0.776 | 0.280 | X | 101403984 | missense variant | C/G | snv | 1.2E-04 | 1.9E-05 | 11 | |
| rs782449839 | 1.000 | 0.160 | X | 101397903 | missense variant | C/G | snv | 8.2E-05 | 1.9E-05 | 1 | |
| rs104894841 | 1.000 | 0.160 | X | 101398907 | stop gained | G/A | snv | 9.5E-06 | 1 | ||
| rs869312262 | 1.000 | 0.160 | X | 101407725 | missense variant | G/A | snv | 9.5E-06 | 1 | ||
| rs797044613 | 1.000 | 0.160 | X | 101407780 | missense variant | T/C;G | snv | 9.4E-06 | 1 | ||
| rs28935493 | 1.000 | 0.160 | X | 101398074 | missense variant | C/T | snv | 9.4E-06 | 1 | ||
| rs28935197 | 0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 | 10 | ||
| rs104894845 | 0.807 | 0.160 | X | 101401752 | missense variant | C/G;T | snv | 5.5E-04 | 8 | ||
| rs104894828 | 0.882 | 0.160 | X | 101398467 | missense variant | C/A;T | snv | 3 | |||
| rs104894851 | 0.925 | 0.200 | X | 101398920 | stop gained | G/T | snv | 3 | |||
| rs104894852 | 0.925 | 0.200 | X | 101397871 | missense variant | T/C | snv | 3 | |||
| rs199473684 | 0.925 | 0.160 | X | 101399747 | 3 prime UTR variant | C/T | snv | 3 | |||
| rs28935485 | 0.925 | 0.160 | X | 101398534 | missense variant | G/C | snv | 3 | |||
| rs28935490 | 1.000 | 0.160 | X | 101398432 | missense variant | C/A;T | snv | 3.0E-03; 5.4E-06 | 3 | ||
| rs398123226 | 0.882 | 0.160 | X | 101398403 | missense variant | G/C;T | snv | 3 | |||
| rs104894830 | 0.925 | 0.160 | X | 101398483 | missense variant | T/C | snv | 2 | |||
| rs104894846 | 0.925 | 0.160 | X | 101398481 | missense variant | C/T | snv | 2 | |||
| rs104894847 | 0.925 | 0.160 | X | 101407846 | missense variant | C/G | snv | 2 | |||
| rs28935195 | 0.925 | 0.200 | X | 101401713 | missense variant | C/T | snv | 2 | |||
| rs397515870 | 1.000 | 0.160 | X | 101400692 | missense variant | G/C;T | snv | 2 |