| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555447012 | 1.000 | 15 | 96332352 | stop gained | G/T | snv | 2 | ||||
| rs1555446983 | 1.000 | 15 | 96332186 | frameshift variant | -/CC | delins | 1 | ||||
| rs201527820 | 1.000 | 15 | 96337611 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 2.8E-05 | 1 | |||
| rs587777371 | 1.000 | 15 | 96337399 | missense variant | C/A | snv | 1 | ||||
| rs587777372 | 1.000 | 15 | 96334247 | missense variant | A/T | snv | 1 | ||||
| rs587777374 | 1.000 | 15 | 96334604 | splice donor variant | G/A | snv | 1 | ||||
| rs780808943 | 1.000 | 15 | 96332314 | inframe insertion | GCAGCA/-;GCA;GCAGCAGCA | delins | 1 |