| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 33 | |
| rs1065489 | 0.695 | 0.440 | 1 | 196740644 | missense variant | G/T | snv | 0.20 | 0.15 | 19 | |
| rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 16 | |
| rs1329428 | 0.807 | 0.160 | 1 | 196733680 | intron variant | C/T | snv | 0.44 | 9 | ||
| rs3753394 | 0.882 | 0.040 | 1 | 196651787 | upstream gene variant | C/T | snv | 0.22 | 5 | ||
| rs2284664 | 0.925 | 0.040 | 1 | 196733395 | intron variant | C/A;T | snv | 3 | |||
| rs779747527 | 1.000 | 0.040 | 6 | 151944292 | frameshift variant | AGCCC/- | del | 1 | |||
| rs776983648 | 1.000 | 0.040 | 11 | 101127885 | missense variant | C/A;G | snv | 4.4E-06 | 1 | ||
| rs61758735 | 1.000 | 0.040 | 12 | 70555234 | missense variant | G/A;T | snv | 5.8E-03; 4.0E-06 | 1 | ||
| rs11865049 | 1.000 | 0.040 | 16 | 87840534 | intron variant | G/A | snv | 6.3E-02 | 1 |