| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs546151500 | 0.925 | 0.080 | 2 | 218643341 | stop gained | G/A;T | snv | 8.0E-06; 4.0E-06 | 5 | ||
| rs1553798675 | 0.925 | 0.080 | 3 | 192335441 | missense variant | C/T | snv | 4 | |||
| rs2486253 | 0.882 | 0.080 | 1 | 160039629 | 3 prime UTR variant | A/C;T | snv | 3 | |||
| rs797044927 | 0.925 | 0.080 | 2 | 165388746 | missense variant | G/A | snv | 3 | |||
| rs7588807 | 0.925 | 0.080 | 2 | 219574380 | intron variant | G/T | snv | 0.48 | 2 | ||
| rs112894280 | 1.000 | 0.080 | 5 | 162093956 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs1569315842 | 1.000 | 0.080 | X | 100408107 | frameshift variant | -/G | delins | 1 |