Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894956 | 1.000 | 0.160 | Y | 2787278 | missense variant | A/G | snv | 1 | |||
| rs104894957 | 1.000 | 0.160 | Y | 2787426 | missense variant | C/G | snv | 1 | |||
| rs104894959 | 0.925 | 0.160 | Y | 2787334 | missense variant | G/C | snv | 1.5E-05 | 1 | ||
| rs104894964 | 1.000 | 0.160 | Y | 2787287 | missense variant | T/A | snv | 1 | |||
| rs104894966 | 0.882 | 0.200 | Y | 2787267 | missense variant | C/T | snv | 1 | |||
| rs104894968 | 1.000 | 0.160 | Y | 2787401 | missense variant | A/G | snv | 1 | |||
| rs104894969 | 1.000 | 0.160 | Y | 2787412 | missense variant | C/T | snv | 1 | |||
| rs104894971 | 0.882 | 0.200 | Y | 2787551 | missense variant | C/T | snv | 4.4E-05 | 1 | ||
| rs104894972 | 0.807 | 0.240 | Y | 2787320 | missense variant | C/T | snv | 1 | |||
| rs104894973 | 1.000 | 0.160 | Y | 2787224 | missense variant | T/A;C | snv | 1 | |||
| rs104894974 | 0.925 | 0.160 | Y | 2787321 | missense variant | C/G | snv | 1 | |||
| rs104894976 | 1.000 | 0.160 | Y | 2787207 | missense variant | G/A | snv | 1 | |||
| rs764249635 | 1.000 | 0.160 | Y | 2787425 | missense variant | A/G | snv | 1.5E-05 | 1 |