| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10230087 | 1.000 | 0.040 | 7 | 114614352 | intron variant | G/A | snv | 0.73 | 2 | ||
| rs12531289 | 1.000 | 0.040 | 7 | 114600061 | intron variant | T/A | snv | 0.73 | 2 | ||
| rs1350135 | 1.000 | 0.040 | 7 | 114602621 | intron variant | C/A;G;T | snv | 2 | |||
| rs2061183 | 1.000 | 0.040 | 7 | 114617959 | intron variant | C/G | snv | 0.73 | 2 | ||
| rs2168351 | 0.851 | 0.120 | 15 | 92440492 | intron variant | A/G | snv | 0.33 | 6 | ||
| rs2279357 | 0.851 | 0.160 | 15 | 74338282 | intron variant | T/C | snv | 0.69 | 5 | ||
| rs3784730 | 0.851 | 0.120 | 15 | 92443898 | intron variant | A/G | snv | 0.44 | 6 | ||
| rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 3 | ||
| rs4307059 | 0.882 | 0.080 | 5 | 25967594 | intron variant | T/A;C | snv | 5 | |||
| rs6551665 | 0.882 | 0.040 | 4 | 61873823 | intron variant | G/A | snv | 0.59 | 4 | ||
| rs199473391 | 1.000 | 0.040 | 12 | 2607117 | stop gained | G/A;T | snv | 2 | |||
| rs397514679 | 0.790 | 0.200 | X | 47574321 | stop gained | G/A | snv | 9 | |||
| rs1163276899 | 1.000 | 0.040 | 3 | 53673125 | missense variant | G/A | snv | 2 | |||
| rs12037377 | 1.000 | 0.040 | 1 | 246551218 | missense variant | G/A | snv | 3.2E-03 | 1.6E-03 | 2 | |
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs121917893 | 0.807 | 0.160 | X | 71167508 | missense variant | C/T | snv | 10 | |||
| rs121918799 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 14 | |
| rs1275980031 | 1.000 | 0.040 | 7 | 103540259 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs141441277 | 0.882 | 0.120 | X | 100689933 | missense variant | G/A | snv | 5.6E-04 | 3.8E-04 | 5 | |
| rs1799793 | 0.557 | 0.640 | 19 | 45364001 | missense variant | C/A;T | snv | 7.1E-06; 0.29 | 72 | ||
| rs201551401 | 0.925 | 0.040 | 7 | 124746694 | missense variant | C/T | snv | 6.4E-05 | 1.4E-05 | 3 | |
| rs28934908 | 0.732 | 0.280 | X | 154031409 | missense variant | G/A;T | snv | 5.5E-06 | 23 | ||
| rs3747333 | 0.925 | 0.040 | X | 5893491 | missense variant | G/A;C;T | snv | 7.6E-03 | 3 | ||
| rs4534 | 0.925 | 0.240 | 8 | 142879686 | missense variant | C/T | snv | 8.4E-02 | 4.1E-02 | 3 | |
| rs4541 | 1.000 | 0.040 | 8 | 142875277 | missense variant | G/A;T | snv | 7.8E-02; 2.0E-05 | 2 |