| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387906788 | 1.000 | 5 | 56856683 | missense variant | T/A;C;G | snv | 2 | ||||
| rs1131692053 | 1.000 | 5 | 56859707 | splice region variant | T/A | snv | 1 | ||||
| rs1131692186 | 1.000 | 5 | 56875105 | missense variant | T/A | snv | 1 | ||||
| rs143853590 | 1.000 | 5 | 56875191 | missense variant | G/A;C;T | snv | 6.1E-04; 1.6E-05; 2.4E-05 | 1 | |||
| rs1554034036 | 1.000 | 5 | 56864915 | missense variant | G/A | snv | 1 | ||||
| rs56160159 | 1.000 | 5 | 56859851 | missense variant | C/T | snv | 5.4E-04 | 1.1E-04 | 1 | ||
| rs886041049 | 1.000 | 5 | 56875268 | missense variant | G/A | snv | 1 |