| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs387907141 | 0.752 | 0.360 | 6 | 157181137 | stop gained | C/T | snv | 24 | |||
| rs147680216 | 0.742 | 0.160 | 2 | 218890244 | missense variant | G/A | snv | 2.1E-03 | 6.9E-04 | 11 | |
| rs142343894 | 0.851 | 0.080 | 1 | 240493250 | missense variant | G/C | snv | 1.7E-03 | 1.8E-03 | 4 | |
| rs481931 | 0.882 | 0.120 | 1 | 94104460 | intron variant | G/T | snv | 0.32 | 3 | ||
| rs116998555 | 0.882 | 0.080 | 2 | 218890118 | missense variant | C/A;T | snv | 4.0E-06; 1.9E-03 | 3 | ||
| rs1325474 | 1.000 | 0.080 | 6 | 83829706 | intergenic variant | G/A | snv | 0.25 | 1 |