| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
| rs104894681 | 0.776 | 0.200 | 19 | 46756793 | missense variant | C/T | snv | 9.0E-06 | 10 | ||
| rs764670582 | 0.827 | 0.120 | 6 | 121447563 | missense variant | G/A | snv | 2.4E-05 | 4.2E-05 | 5 | |
| rs137853128 | 0.925 | 0.080 | 17 | 72121618 | missense variant | C/A | snv | 2 | |||
| rs28940282 | 0.925 | 0.080 | 17 | 72122780 | missense variant | C/T | snv | 2 | |||
| rs587776541 | 0.925 | 0.200 | 17 | 72123592 | frameshift variant | -/C | delins | 2 | |||
| rs80338688 | 0.925 | 0.200 | 17 | 72124177 | stop gained | C/A;G;T | snv | 3.3E-04 | 2 | ||
| rs866706988 | 0.925 | 0.200 | 17 | 72122795 | missense variant | C/A;T | snv | 2 | |||
| rs104894647 | 0.925 | 0.080 | 17 | 72122804 | missense variant | A/G | snv | 2 | |||
| rs137853130 | 0.925 | 0.200 | 17 | 72122759 | missense variant | G/A | snv | 2 | |||
| rs1057518669 | 1.000 | 0.080 | 17 | 72124284 | missense variant | T/C | snv | 1 | |||
| rs137853129 | 1.000 | 0.080 | 17 | 72122749 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs1555629022 | 1.000 | 0.080 | 17 | 72121643 | stop gained | C/G | snv | 1 | |||
| rs1555629037 | 1.000 | 0.080 | 17 | 72121740 | stop gained | C/T | snv | 1 | |||
| rs1555629443 | 1.000 | 0.080 | 17 | 72124229 | stop gained | C/T | snv | 1 | |||
| rs1567910689 | 1.000 | 0.080 | 17 | 72122778 | missense variant | A/C | snv | 1 | |||
| rs1057518216 | 1.000 | 0.080 | 17 | 72124037 | stop gained | C/A;T | snv | 1 | |||
| rs1131691554 | 1.000 | 0.080 | 17 | 72122796 | missense variant | C/T | snv | 1 | |||
| rs1407667250 | 1.000 | 0.080 | 17 | 72121727 | missense variant | C/A | snv | 1 | |||
| rs1555629158 | 1.000 | 0.080 | 17 | 72122802 | missense variant | A/G | snv | 1 |