| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7709505 | 0.925 | 0.040 | 5 | 91261401 | intron variant | A/C;T | snv | 2 | |||
| rs2367281 | 5 | 91107358 | intron variant | C/A;T | snv | 1 | |||||
| rs796051865 | 1.000 | 0.200 | 5 | 91153324 | frameshift variant | TGGCCAGGGGTCACTGATA/- | delins | 1 | |||
| rs140935700 | 5 | 91316148 | upstream gene variant | G/A | snv | 9.4E-03 | 1 | ||||
| rs13357230 | 5 | 91115255 | intron variant | A/G | snv | 5.8E-02 | 1 | ||||
| rs4489092 | 5 | 91124827 | intron variant | G/T | snv | 0.49 | 1 | ||||
| rs59661306 | 1.000 | 0.080 | 5 | 91087644 | intron variant | A/G | snv | 0.18 | 1 |