Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121909300 | 1.000 | 0.040 | 5 | 41749579 | missense variant | C/A | snv | 1 | |||
| rs121909301 | 1.000 | 0.040 | 5 | 41803148 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs121909302 | 1.000 | 0.040 | 5 | 41842690 | missense variant | C/T | snv | 1 | |||
| rs121909303 | 1.000 | 0.040 | 5 | 41842685 | missense variant | C/T | snv | 2.4E-05 | 2.1E-05 | 1 | |
| rs1327401976 | 1.000 | 0.040 | 5 | 41749544 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs201752548 | 1.000 | 0.040 | 5 | 41842702 | missense variant | G/A | snv | 1.6E-05 | 1 | ||
| rs267606930 | 1.000 | 0.040 | 5 | 41853435 | missense variant | A/T | snv | 1 | |||
| rs368841359 | 1.000 | 0.040 | 5 | 41840506 | missense variant | C/A;T | snv | 4.0E-06 | 1 |