Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1411331203 | 1.000 | 0.080 | 1 | 173914564 | missense variant | G/T | snv | 7.0E-06 | 1 | ||
| rs1423630663 | 1.000 | 0.080 | 1 | 173910764 | missense variant | A/G | snv | 1 | |||
| rs1425532034 | 1.000 | 0.080 | 1 | 173911830 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
| rs147266200 | 1.000 | 0.080 | 1 | 173914696 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs28929469 | 1.000 | 0.080 | 1 | 173914795 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs387906575 | 1.000 | 0.080 | 1 | 173914893 | missense variant | A/G | snv | 1 | |||
| rs483352854 | 1.000 | 0.080 | 1 | 173910875 | missense variant | G/T | snv | 1 | |||
| rs758087836 | 1.000 | 0.080 | 1 | 173909900 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs765445413 | 1.000 | 0.080 | 1 | 173911974 | missense variant | T/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs907768931 | 1.000 | 0.080 | 1 | 173914677 | missense variant | T/C | snv | 7.0E-06 | 1 |