Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894492 | 1.000 | 0.160 | 15 | 71811590 | missense variant | C/A;T | snv | 1.3E-05; 3.0E-05; 4.4E-06 | 2.8E-05 | 1 | |
| rs104894493 | 1.000 | 0.160 | 15 | 71811591 | missense variant | G/A | snv | 2.0E-04 | 3.1E-04 | 1 | |
| rs1278137915 | 1.000 | 0.160 | 15 | 71811783 | missense variant | G/A;T | snv | 1 | |||
| rs1303613101 | 1.000 | 0.160 | 15 | 71817671 | missense variant | T/A;C | snv | 8.1E-06; 4.0E-06 | 1 | ||
| rs146403122 | 0.925 | 0.160 | 15 | 71811966 | missense variant | G/A | snv | 4.3E-03 | 1.8E-03 | 1 | |
| rs1489149705 | 1.000 | 0.160 | 15 | 71811810 | missense variant | G/A | snv | 2.1E-05 | 1 | ||
| rs28937873 | 0.807 | 0.160 | 15 | 71813573 | missense variant | G/A | snv | 4.0E-04 | 3.1E-04 | 1 | |
| rs377257254 | 1.000 | 0.160 | 15 | 71813408 | missense variant | C/A;T | snv | 3.7E-05; 2.1E-05 | 1 | ||
| rs752883545 | 1.000 | 0.160 | 15 | 71814024 | missense variant | T/C | snv | 8.2E-06 | 7.0E-06 | 1 | |
| rs766769900 | 1.000 | 0.160 | 15 | 71817605 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs774102273 | 1.000 | 0.160 | 15 | 71813566 | missense variant | C/G;T | snv | 4.1E-06; 8.2E-06 | 1 | ||
| rs990307718 | 1.000 | 0.160 | 15 | 71811830 | missense variant | C/T | snv | 2.0E-05 | 7.0E-06 | 1 |