| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913595 | 0.742 | 0.160 | 1 | 161306785 | missense variant | G/A;T | snv | 11 | |||
| rs121913586 | 0.752 | 0.200 | 1 | 161306414 | missense variant | C/G;T | snv | 10 | |||
| rs104894621 | 0.790 | 0.080 | 17 | 15239575 | missense variant | G/A | snv | 9 | |||
| rs104894158 | 0.851 | 0.080 | 10 | 62813835 | missense variant | A/T | snv | 5 | |||
| rs281865137 | 0.851 | 0.080 | 10 | 62813496 | missense variant | C/T | snv | 4 | |||
| rs797044845 | 0.882 | 0.080 | 1 | 161307311 | missense variant | C/T | snv | 3 | |||
| rs74315521 | 0.882 | 0.120 | 22 | 37974148 | stop gained | G/A | snv | 3 | |||
| rs757078088 | 1.000 | 0.080 | 10 | 62815875 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs1244845760 | 1.000 | 0.080 | 1 | 10295763 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1430414164 | 1.000 | 0.080 | 6 | 43636404 | missense variant | G/A | snv | 1 |