| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs374997012 | 0.851 | 0.280 | 10 | 100989114 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 9 | |
| rs886037832 | 0.851 | 0.280 | 10 | 100988541 | frameshift variant | T/- | delins | 9 | |||
| rs863223921 | 0.925 | 0.280 | 10 | 100989406 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs80356543 | 0.925 | 0.240 | 10 | 100989165 | missense variant | A/C;G | snv | 2 | |||
| rs80356542 | 1.000 | 0.080 | 10 | 100989162 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs386834145 | 1.000 | 0.080 | 10 | 100989766 | missense variant | C/G | snv | 1 | |||
| rs386834146 | 1.000 | 0.080 | 10 | 100989787 | missense variant | C/G;T | snv | 8.0E-06 | 1 | ||
| rs80356540 | 1.000 | 0.080 | 10 | 100990474 | missense variant | A/G | snv | 2.5E-04 | 2.7E-04 | 1 | |
| rs80356541 | 1.000 | 0.080 | 10 | 100989687 | synonymous variant | C/T | snv | 1 | |||
| rs80356544 | 1.000 | 0.080 | 10 | 100989770 | missense variant | C/T | snv | 1.4E-05 | 1 |