| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs367737727 | 1.000 | 0.080 | 14 | 100128600 | missense variant | C/T | snv | 1.1E-05 | 1 | ||
| rs773205136 | 1.000 | 0.080 | 2 | 100294302 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
| rs367898512 | 1.000 | 0.080 | 10 | 101002900 | missense variant | G/A | snv | 2.8E-05 | 7.0E-06 | 1 | |
| rs369664812 | 1.000 | 0.080 | 7 | 101223799 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 | 1 | |
| rs2186607 | 0.776 | 0.080 | 11 | 101785666 | intron variant | T/A | snv | 0.51 | 10 | ||
| rs990101456 | 1.000 | 0.080 | 10 | 102109138 | missense variant | C/T | snv | 1 | |||
| rs1287689842 | 1.000 | 0.080 | 7 | 102281843 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs6214 | 0.672 | 0.400 | 12 | 102399791 | 3 prime UTR variant | C/T | snv | 0.45 | 1 | ||
| rs3774959 | 0.925 | 0.080 | 4 | 102589957 | intron variant | G/A | snv | 0.34 | 1 | ||
| rs4450168 | 0.790 | 0.080 | 11 | 10265208 | intron variant | A/C;T | snv | 0.12 | 9 | ||
| rs4919687 | 0.742 | 0.160 | 10 | 102835491 | non coding transcript exon variant | G/A | snv | 0.25 | 9 | ||
| rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 2 | |
| rs2276109 | 0.701 | 0.440 | 11 | 102875061 | upstream gene variant | T/C | snv | 9.2E-02 | 2 | ||
| rs12548629 | 0.776 | 0.120 | 8 | 103189173 | intron variant | C/T | snv | 0.24 | 10 | ||
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs141752671 | 0.708 | 0.280 | 11 | 103745837 | intron variant | A/G | snv | 5.4E-03 | 17 | ||
| rs148883465 | 0.708 | 0.280 | 11 | 103813371 | intron variant | A/G | snv | 7.2E-03 | 17 | ||
| rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs189206655 | 1.000 | 0.080 | 9 | 104809521 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs314277 | 0.925 | 0.080 | 6 | 104959787 | intron variant | A/C;G;T | snv | 4 | |||
| rs17035289 | 0.790 | 0.080 | 4 | 105127134 | intergenic variant | T/C | snv | 0.25 | 9 | ||
| rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 25 | ||
| rs17035310 | 0.790 | 0.080 | 4 | 105143597 | upstream gene variant | C/T | snv | 0.14 | 10 | ||
| rs1391441 | 0.763 | 0.240 | 4 | 105207603 | intron variant | G/A | snv | 0.70 | 10 | ||
| rs371981699 | 1.000 | 0.080 | 14 | 105217692 | missense variant | C/T | snv | 4.0E-05 | 4.2E-05 | 1 |