| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
| rs1167827 | 7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 | 5 | ||||
| rs2764261 | 6 | 108606639 | intron variant | A/G;T | snv | 3 | |||||
| rs6870983 | 5 | 88401716 | intron variant | C/T | snv | 0.29 | 3 |