| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ||
| rs786205066 | 1.000 | 0.120 | 15 | 68211258 | splice region variant | C/A | snv | 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 | ||
| rs397515352 | 0.925 | 0.120 | 15 | 68211844 | frameshift variant | -/G | delins | 2.4E-05; 2.8E-05 | 3 | ||
| rs121908080 | 0.925 | 0.120 | 15 | 68211698 | inframe deletion | ATG/- | delins | 2 | |||
| rs768422260 | 0.925 | 0.120 | 15 | 68208280 | inframe deletion | GAG/- | delins | 1.4E-05 | 2 | ||
| rs774543080 | 0.925 | 0.120 | 15 | 68211765 | frameshift variant | AG/- | delins | 8.0E-06 | 2 | ||
| rs121908079 | 1.000 | 0.120 | 15 | 68211289 | inframe deletion | ATA/- | delins | 1 | |||
| rs154774639 | 1.000 | 0.120 | 15 | 68208186 | frameshift variant | G/- | delins | 1.4E-05 | 1 | ||
| rs1555438229 | 1.000 | 0.120 | 15 | 68208288 | frameshift variant | -/AG | delins | 1 | |||
| rs1555438234 | 1.000 | 0.120 | 15 | 68208306 | frameshift variant | TGTCC/- | delins | 1 | |||
| rs1567095153 | 1.000 | 0.120 | 15 | 68209749 | frameshift variant | -/G | delins | 1 | |||
| rs762902907 | 1.000 | 0.120 | 15 | 68211306 | frameshift variant | -/A | delins | 4.0E-06 | 7.0E-06 | 1 | |
| rs786205065 | 1.000 | 0.120 | 15 | 68229578 | frameshift variant | C/- | delins | 1 | |||
| rs786205067 | 1.000 | 0.120 | 15 | 68214315 | frameshift variant | -/CGTT | delins | 1 |