| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs771866012 | 0.882 | 0.080 | 10 | 72007522 | missense variant | C/G;T | snv | 4.2E-06; 4.2E-06 | 8 | ||
| rs1316347883 | 0.851 | 0.080 | 10 | 72007935 | missense variant | G/A;C | snv | 6.9E-06 | 4 | ||
| rs769540174 | 1.000 | 0.080 | 10 | 72007559 | frameshift variant | G/-;GG | delins | 4 | |||
| rs121908616 | 1.000 | 0.080 | 10 | 72007807 | missense variant | T/C | snv | 1 | |||
| rs121908617 | 1.000 | 0.080 | 10 | 72007695 | missense variant | C/A;T | snv | 1 | |||
| rs121908618 | 1.000 | 0.080 | 10 | 72007951 | missense variant | T/C | snv | 1 | |||
| rs121908619 | 1.000 | 0.080 | 10 | 72007634 | stop gained | C/A;T | snv | 1 | |||
| rs121908620 | 0.925 | 0.080 | 10 | 72007888 | missense variant | T/C | snv | 1 | |||
| rs1416783446 | 1.000 | 0.080 | 10 | 72008343 | stop gained | C/T | snv | 5.7E-06 | 1 | ||
| rs1554817549 | 1.000 | 0.080 | 10 | 72007711 | missense variant | C/G | snv | 1 | |||
| rs267606732 | 1.000 | 0.080 | 10 | 72008019 | stop gained | C/A;T | snv | 1 | |||
| rs267606733 | 1.000 | 0.080 | 10 | 72007512 | missense variant | C/G;T | snv | 1 | |||
| rs267606734 | 1.000 | 0.080 | 10 | 72008145 | missense variant | G/A | snv | 1 | |||
| rs267606735 | 1.000 | 0.080 | 10 | 72007453 | missense variant | C/A;T | snv | 4.3E-06; 4.3E-06 | 1 | ||
| rs28937593 | 1.000 | 0.080 | 10 | 72007942 | missense variant | G/A | snv | 1 | |||
| rs747171013 | 1.000 | 0.080 | 10 | 72008094 | missense variant | G/A;T | snv | 1 |