| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057523354 | 0.763 | 0.480 | 13 | 110179387 | missense variant | C/A | snv | 13 | |||
| rs118204456 | 0.851 | 0.200 | 5 | 177404231 | missense variant | G/C;T | snv | 4.3E-06 | 7 | ||
| rs1554995260 | 1.000 | 0.120 | 11 | 57602098 | frameshift variant | -/T | delins | 3 | |||
| rs9833094 | 1.000 | 0.080 | 3 | 100872081 | intron variant | C/A;T | snv | 2 | |||
| rs9323624 | 1.000 | 0.080 | 14 | 76033960 | intron variant | T/C | snv | 0.50 | 2 | ||
| rs889957249 | 1.000 | 0.160 | 6 | 160718730 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs978962357 | 11 | 57614553 | missense variant | T/C | snv | 4.0E-06 | 1 | ||||
| rs1057519445 | 11 | 85734436 | frameshift variant | C/- | del | 1 |