Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs66501246 | 0.925 | 0.120 | 17 | 50195441 | missense variant | C/G;T | snv | 2 | |||
| rs66527965 | 0.763 | 0.240 | 17 | 50193038 | missense variant | C/A;T | snv | 2 | |||
| rs67507747 | 0.827 | 0.160 | 17 | 50194032 | missense variant | C/A;G;T | snv | 2 | |||
| rs67682641 | 0.807 | 0.240 | 17 | 50194375 | missense variant | C/A;T | snv | 2 | |||
| rs72654795 | 0.925 | 0.120 | 17 | 50188565 | missense variant | C/T | snv | 2 | |||
| rs66721653 | 1.000 | 17 | 50195665 | missense variant | C/A;T | snv | 1 | ||||
| rs67182491 | 1.000 | 17 | 50195575 | missense variant | C/A;T | snv | 1 | ||||
| rs67693970 | 0.882 | 0.120 | 17 | 50190099 | missense variant | C/G;T | snv | 1 | |||
| rs68114505 | 1.000 | 17 | 50191814 | missense variant | C/A;T | snv | 1 | ||||
| rs72645321 | 0.925 | 0.120 | 17 | 50197045 | missense variant | C/T | snv | 1 | |||
| rs72645357 | 0.776 | 0.240 | 17 | 50196163 | missense variant | C/T | snv | 1 | |||
| rs72645365 | 0.925 | 0.120 | 17 | 50195656 | missense variant | C/A | snv | 1 | |||
| rs72648322 | 1.000 | 17 | 50195330 | missense variant | C/A;T | snv | 1 | ||||
| rs72648353 | 1.000 | 17 | 50194384 | missense variant | C/A | snv | 1 | ||||
| rs72651636 | 1.000 | 17 | 50191868 | missense variant | C/T | snv | 1 | ||||
| rs72653131 | 0.882 | 0.120 | 17 | 50190045 | missense variant | C/T | snv | 1 | |||
| rs72653169 | 1.000 | 17 | 50188920 | missense variant | C/T | snv | 1 | ||||
| rs72653170 | 0.752 | 0.240 | 17 | 50188908 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs72654796 | 1.000 | 17 | 50188556 | missense variant | C/T | snv | 1 |