| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555440206 | 1.000 | 0.120 | 15 | 68229584 | start lost | T/C | snv | 1 | |||
| rs1567095153 | 1.000 | 0.120 | 15 | 68209749 | frameshift variant | -/G | delins | 1 | |||
| rs1567096598 | 1.000 | 0.120 | 15 | 68214337 | missense variant | A/T | snv | 1 | |||
| rs374681194 | 1.000 | 0.120 | 15 | 68208321 | missense variant | C/A;T | snv | 2.0E-04 | 1 | ||
| rs553192210 | 1.000 | 0.120 | 15 | 68214177 | non coding transcript exon variant | C/A;G | snv | 2.8E-05 | 1 | ||
| rs746753722 | 1.000 | 0.120 | 15 | 68208397 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs747229909 | 1.000 | 0.120 | 15 | 68211716 | missense variant | G/A;C | snv | 5.6E-05 | 1 | ||
| rs758921701 | 1.000 | 0.120 | 15 | 68208180 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs762902907 | 1.000 | 0.120 | 15 | 68211306 | frameshift variant | -/A | delins | 4.0E-06 | 7.0E-06 | 1 | |
| rs763944821 | 1.000 | 0.120 | 15 | 68229536 | missense variant | C/T | snv | 8.2E-04 | 9.8E-05 | 1 | |
| rs764571295 | 1.000 | 0.120 | 15 | 68209640 | missense variant | T/C;G | snv | 1.6E-05; 2.4E-05 | 1 | ||
| rs786205065 | 1.000 | 0.120 | 15 | 68229578 | frameshift variant | C/- | delins | 1 | |||
| rs786205066 | 1.000 | 0.120 | 15 | 68211258 | splice region variant | C/A | snv | 1 | |||
| rs786205067 | 1.000 | 0.120 | 15 | 68214315 | frameshift variant | -/CGTT | delins | 1 | |||
| rs919850756 | 1.000 | 0.120 | 15 | 68211685 | missense variant | G/A | snv | 1 | |||
| rs959199004 | 1.000 | 0.120 | 15 | 68208376 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs587779408 | 0.882 | 0.160 | 11 | 6391804 | missense variant | G/A | snv | 2.4E-05 | 2.8E-05 | 3 |