Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28935490 | 1.000 | 0.160 | X | 101398432 | missense variant | C/A;T | snv | 3.0E-03; 5.4E-06 | 1 | ||
| rs104894845 | 0.807 | 0.160 | X | 101401752 | missense variant | C/G;T | snv | 5.5E-04 | 1 | ||
| rs140329381 | 1.000 | 0.160 | X | 101398504 | missense variant | T/A;C | snv | 1.6E-04 | 1 | ||
| rs104894833 | 0.776 | 0.280 | X | 101403984 | missense variant | C/G | snv | 1.2E-04 | 1.9E-05 | 1 | |
| rs782449839 | 1.000 | 0.160 | X | 101397903 | missense variant | C/G | snv | 8.2E-05 | 1.9E-05 | 1 | |
| 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 | |
| rs869312163 | 1.000 | 0.160 | X | 101398032 | missense variant | C/G;T | snv | 1.1E-05 | 1 | ||
| rs372966991 | 1.000 | 0.160 | X | 101403845 | missense variant | C/A;T | snv | 1.1E-05 | 1 | ||
| rs869312344 | 1.000 | 0.160 | X | 101400700 | missense variant | C/G;T | snv | 5.5E-06 | 1 | ||
| rs782197638 | 1.000 | 0.160 | X | 101403819 | missense variant | C/T | snv | 5.5E-06 | 1 | ||
| rs869312162 | 1.000 | 0.160 | X | 101398044 | missense variant | G/C | snv | 5.5E-06 | 1 | ||
| rs782598150 | 1.000 | 0.160 | X | 101398021 | missense variant | C/A;G | snv | 5.5E-06 | 1 | ||
| rs28935197 | 0.776 | 0.280 | X | 101398942 | missense variant | T/C | snv | 5.5E-06 | 1 | ||
| rs190347120 | 1.000 | 0.160 | X | 101398796 | missense variant | C/A;T | snv | 5.5E-06 | 1 | ||
| rs397515874 | 1.000 | 0.160 | X | 101398857 | missense variant | C/G;T | snv | 5.5E-06 | 1 | ||
| rs104894827 | 1.000 | 0.160 | X | 101398033 | missense variant | G/A | snv | 1 | |||
| rs104894828 | 0.882 | 0.160 | X | 101398467 | missense variant | C/A;T | snv | 1 | |||
| rs104894830 | 0.925 | 0.160 | X | 101398483 | missense variant | T/C | snv | 1 | |||
| rs104894831 | 1.000 | 0.160 | X | 101407786 | missense variant | G/A | snv | 1 | |||
| rs104894832 | 1.000 | 0.160 | X | 101398387 | missense variant | C/G;T | snv | 1 | |||
| rs104894834 | 1.000 | 0.160 | X | 101403846 | missense variant | G/A | snv | 1 | |||
| rs104894835 | 1.000 | 0.160 | X | 101407803 | missense variant | T/C | snv | 1 | |||
| rs104894836 | 1.000 | 0.160 | X | 101407738 | missense variant | A/C | snv | 1 | |||
| rs104894837 | 1.000 | 0.160 | X | 101401743 | missense variant | G/A | snv | 1 |