| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7626962 | 0.790 | 0.080 | 3 | 38579416 | missense variant | G/A;T | snv | 1.6E-05; 5.9E-03 | 10 | ||
| rs121918600 | 0.882 | 0.080 | 1 | 237791441 | missense variant | C/T | snv | 5 | |||
| rs1860561 | 0.851 | 0.080 | 12 | 110345436 | intron variant | G/A | snv | 0.19 | 5 | ||
| rs59301204 | 0.925 | 0.080 | 1 | 156135956 | missense variant | G/A;C | snv | 1.2E-05 | 4 | ||
| rs121918604 | 0.882 | 0.080 | 1 | 237798037 | missense variant | G/A;T | snv | 1.7E-05 | 3 | ||
| rs1266360671 | 0.925 | 0.080 | 1 | 237270518 | missense variant | T/C | snv | 4.7E-06 | 3 | ||
| rs1805120 | 0.882 | 0.080 | 7 | 150952443 | synonymous variant | G/A | snv | 0.30 | 0.26 | 3 | |
| rs192749597 | 0.882 | 0.080 | 12 | 2679712 | missense variant | C/T | snv | 9.2E-04 | 3.5E-03 | 3 | |
| rs755373114 | 0.925 | 0.080 | 4 | 113341742 | missense variant | A/C | snv | 7.2E-05 | 3 | ||
| rs761056344 | 0.925 | 0.080 | 6 | 118558994 | missense variant | C/G;T | snv | 4.0E-06; 3.2E-05 | 3 | ||
| rs1049194905 | 0.925 | 0.080 | 3 | 38604063 | synonymous variant | A/G | snv | 2 | |||
| rs1237080661 | 0.925 | 0.080 | 3 | 38604780 | stop gained | A/G;T | snv | 2.8E-05 | 2 | ||
| rs1355262401 | 1.000 | 0.080 | 6 | 121447691 | missense variant | T/G | snv | 7.0E-06 | 2 | ||
| rs1554108172 | 0.925 | 0.080 | 6 | 7579983 | stop gained | G/T | snv | 2 | |||
| rs184934308 | 0.925 | 0.080 | 3 | 38575342 | synonymous variant | G/A | snv | 4.1E-04 | 9.1E-05 | 2 | |
| rs201698592 | 0.925 | 0.080 | 11 | 2847916 | synonymous variant | C/T | snv | 1.7E-04 | 2.8E-05 | 2 | |
| rs740952 | 0.925 | 0.080 | 7 | 150952515 | synonymous variant | G/A;T | snv | 0.30; 7.2E-05 | 2 | ||
| rs750678689 | 0.925 | 0.080 | 3 | 38566466 | synonymous variant | G/A | snv | 8.0E-06 | 2.1E-05 | 2 | |
| rs764772142 | 0.925 | 0.080 | 1 | 237377349 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||
| rs765835441 | 1.000 | 0.080 | 1 | 237726291 | missense variant | C/T | snv | 2.7E-05 | 2.1E-05 | 1 | |
| rs45546039 | 0.732 | 0.120 | 3 | 38613781 | missense variant | C/A;T | snv | 4.1E-06 | 15 | ||
| rs120074192 | 0.763 | 0.120 | 11 | 2527959 | missense variant | A/G | snv | 10 | |||
| rs3745297 | 0.790 | 0.120 | 19 | 49154952 | missense variant | A/C | snv | 0.41 | 0.38 | 10 | |
| rs794728708 | 0.827 | 0.120 | 1 | 237377386 | missense variant | G/A;T | snv | 8 | |||
| rs199473605 | 0.851 | 0.120 | 3 | 38560374 | missense variant | C/G;T | snv | 4.8E-05; 4.0E-06 | 7 |