| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1340513 | 0.882 | 0.120 | 9 | 6977633 | intron variant | G/A | snv | 0.75 | 4 | ||
| rs1350135 | 1.000 | 0.040 | 7 | 114602621 | intron variant | C/A;G;T | snv | 2 | |||
| rs1372713010 | 1.000 | 0.040 | 1 | 151428041 | missense variant | G/A | snv | 1 | |||
| rs1390938 | 0.807 | 0.200 | 8 | 20179202 | missense variant | A/G | snv | 0.71 | 0.78 | 7 | |
| rs1396313317 | 1.000 | 0.040 | 7 | 147562137 | splice acceptor variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs139896303 | 1.000 | 0.040 | 12 | 71972584 | missense variant | G/A | snv | 1.2E-04 | 5.6E-05 | 1 | |
| rs141441277 | 0.882 | 0.120 | X | 100689933 | missense variant | G/A | snv | 5.6E-04 | 3.8E-04 | 5 | |
| rs141560292 | 1.000 | 0.040 | 1 | 162154408 | missense variant | G/A | snv | 1.6E-05 | 7.7E-05 | 1 | |
| rs1418634444 | 1.000 | 0.040 | 1 | 151408777 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
| rs1452048149 | 1.000 | 0.040 | 1 | 151404828 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1452075 | 1.000 | 0.040 | 3 | 62495388 | intron variant | C/T | snv | 0.73 | 4 | ||
| rs1460808228 | 0.851 | 0.040 | 16 | 24185518 | missense variant | T/C | snv | 7.0E-06 | 4 | ||
| rs1476293577 | 1.000 | 0.040 | 1 | 151428188 | missense variant | G/A;C | snv | 1 | |||
| rs1477437491 | 0.925 | 0.040 | 1 | 162367213 | missense variant | G/A | snv | 2.8E-05 | 2 | ||
| rs1484207450 | 1.000 | 0.040 | 1 | 151405155 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs1488545 | 1.000 | 0.040 | 3 | 173765644 | intron variant | C/A | snv | 0.80 | 1 | ||
| rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
| rs1553518509 | 1.000 | 0.040 | 2 | 148468916 | stop gained | C/T | snv | 2 | |||
| rs1555910143 | 0.925 | 0.120 | 22 | 50721257 | frameshift variant | CT/- | del | 2 | |||
| rs1557863430 | 1.000 | 0.040 | 1 | 151405229 | missense variant | T/C | snv | 1 | |||
| rs1557863440 | 1.000 | 0.040 | 1 | 151405233 | missense variant | T/C | snv | 1 | |||
| rs1557863546 | 1.000 | 0.040 | 1 | 151405263 | missense variant | T/A | snv | 1 | |||
| rs1557867853 | 1.000 | 0.040 | 1 | 151406330 | missense variant | G/A | snv | 1 | |||
| rs1557870645 | 1.000 | 0.040 | 1 | 151407271 | missense variant | C/T | snv | 1 | |||
| rs1557874046 | 1.000 | 0.040 | 1 | 151408807 | missense variant | T/G | snv | 1 |