| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893950 | 0.925 | 0.080 | 6 | 145627691 | stop gained | G/A;C | snv | 7.7E-05 | 2 | ||
| rs1554263366 | 1.000 | 0.040 | 6 | 145686284 | missense variant | T/C | snv | 1 | |||
| rs781291421 | 1.000 | 0.040 | 6 | 145635468 | stop gained | C/A;T | snv | 1.2E-05; 2.8E-05 | 1 | ||
| rs587776553 | 1.000 | 0.080 | 6 | 145686262 | stop gained | -/T | delins | 1 | |||
| rs137852917 | 1.000 | 0.080 | 6 | 145627577 | missense variant | C/A;T | snv | 8.0E-06; 1.2E-05 | 1 | ||
| rs137852915 | 1.000 | 0.080 | 6 | 145686276 | missense variant | G/A | snv | 2.4E-05 | 7.0E-06 | 1 | |
| rs587776554 | 1.000 | 0.080 | 6 | 145627458 | frameshift variant | -/A | delins | 1 | |||
| rs104893955 | 1.000 | 0.080 | 6 | 145735405 | missense variant | A/C;T | snv | 1 |