| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
| rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 10 | ||
| rs199473062 | 0.827 | 0.120 | 3 | 38622401 | stop gained | C/A;G;T | snv | 4.1E-06 | 5 | ||
| rs104894485 | 0.882 | 0.080 | 15 | 73325378 | missense variant | C/T | snv | 3.6E-05 | 7.0E-06 | 4 | |
| rs6817105 | 0.882 | 0.080 | 4 | 110784612 | intergenic variant | T/C | snv | 0.19 | 3 | ||
| rs768138092 | 0.925 | 0.080 | 3 | 158105927 | missense variant | G/C;T | snv | 4.3E-06; 4.3E-06 | 2 | ||
| rs1474925551 | 1.000 | 0.080 | 2 | 154699081 | missense variant | G/C | snv | 1 |