Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1170430756 | 1.000 | 0.080 | 1 | 173911987 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
| rs121909547 | 1.000 | 0.080 | 1 | 173914726 | missense variant | G/A;T | snv | 4.8E-05 | 1 | ||
| rs121909551 | 1.000 | 0.080 | 1 | 173914743 | missense variant | G/A | snv | 8.2E-04 | 9.0E-04 | 1 | |
| rs121909552 | 0.925 | 0.080 | 1 | 173914725 | missense variant | C/T | snv | 9.5E-05 | 1.7E-04 | 1 | |
| rs121909558 | 1.000 | 0.080 | 1 | 173914845 | missense variant | A/T | snv | 1 | |||
| rs121909563 | 1.000 | 0.080 | 1 | 173911941 | missense variant | C/A;T | snv | 1.6E-05; 4.0E-06 | 1 | ||
| rs121909565 | 1.000 | 0.080 | 1 | 173909564 | missense variant | A/G | snv | 1 | |||
| rs121909567 | 0.925 | 0.120 | 1 | 173914570 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs121909569 | 1.000 | 0.080 | 1 | 173911981 | missense variant | A/G | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs121909571 | 1.000 | 0.080 | 1 | 173910861 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs121909572 | 1.000 | 0.080 | 1 | 173910849 | missense variant | A/G | snv | 1 | |||
| rs121909573 | 1.000 | 0.080 | 1 | 173914582 | missense variant | A/G | snv | 1 | |||
| 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 | ||
| rs1188571702 | 1.000 | 0.080 | 1 | 173903962 | missense variant | A/G | snv | 1 | |||
| rs121909546 | 1.000 | 0.080 | 1 | 173903978 | missense variant | C/T | snv | 1 | |||
| rs121909548 | 1.000 | 0.080 | 1 | 173904038 | missense variant | C/A;G | snv | 8.9E-04 | 1 |