| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
| rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
| rs1232880706 | 0.689 | 0.440 | 15 | 48526247 | stop gained | C/A;T | snv | 36 | |||
| rs1561892336 | 0.807 | 0.200 | 6 | 43050050 | stop gained | C/T | snv | 13 | |||
| rs1561881909 | 0.925 | 0.200 | 6 | 43044835 | frameshift variant | G/- | delins | 9 | |||
| rs1561898352 | 0.882 | 0.200 | 6 | 43052582 | frameshift variant | -/A | delins | 8 |