| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs207016 | 1.000 | 0.040 | 21 | 17270927 | intergenic variant | G/A | snv | 1.00 | 1 | ||
| rs7854303 | 1.000 | 0.200 | 9 | 5557672 | missense variant | T/C | snv | 1.00 | 1.00 | 1 | |
| rs659497 | 1.000 | 0.120 | 17 | 42537437 | synonymous variant | T/C | snv | 0.99 | 0.99 | 1 | |
| rs2738780 | 0.882 | 0.080 | 20 | 63668461 | intron variant | T/C | snv | 0.99 | 3 | ||
| rs616338 | 0.925 | 0.080 | 17 | 49219935 | missense variant | T/C | snv | 0.99 | 0.99 | 2 | |
| rs6264 | 0.925 | 0.040 | 7 | 50544037 | missense variant | T/C | snv | 1.00 | 0.99 | 2 | |
| rs1187120 | 0.925 | 0.040 | 6 | 34182850 | intergenic variant | T/C | snv | 0.99 | 3 | ||
| rs672961 | 1.000 | 0.040 | 1 | 70101505 | intron variant | C/G | snv | 0.99 | 1 | ||
| rs223469 | 1.000 | 0.040 | 4 | 102778621 | intergenic variant | T/C | snv | 0.99 | 1 | ||
| rs1169305 | 1.000 | 0.040 | 12 | 120999579 | missense variant | A/G | snv | 1.00 | 0.99 | 2 | |
| rs25655 | 0.925 | 0.080 | 1 | 223712706 | missense variant | C/G | snv | 1.00 | 0.99 | 2 | |
| rs220733 | 1.000 | 0.080 | 6 | 159897771 | intron variant | A/C;G | snv | 0.99 | 3 | ||
| rs4844609 | 1.000 | 0.080 | 1 | 207609571 | missense variant | A/T | snv | 0.99 | 0.99 | 1 | |
| rs10282312 | 1.000 | 0.120 | 7 | 143320714 | missense variant | G/T | snv | 0.99 | 0.98 | 1 | |
| rs429699 | 0.925 | 0.080 | 5 | 1409012 | intron variant | T/C | snv | 0.96 | 0.98 | 3 | |
| rs1473418 | 1.000 | 0.080 | 18 | 63319316 | 5 prime UTR variant | C/G | snv | 0.98 | 2 | ||
| rs2857461 | 0.882 | 0.160 | 22 | 29272015 | intron variant | C/T | snv | 0.98 | 3 | ||
| rs1529927 | 1.000 | 0.040 | 16 | 56870675 | missense variant | C/G | snv | 1.6E-05; 0.98 | 0.98 | 1 | |
| rs2747648 | 0.925 | 0.080 | 6 | 152101200 | 3 prime UTR variant | C/T | snv | 0.98 | 2 | ||
| rs6441600 | 1.000 | 0.040 | 3 | 93956895 | intron variant | C/G | snv | 0.97 | 1 | ||
| rs6472812 | 1.000 | 0.080 | 8 | 74004849 | missense variant | A/G | snv | 0.97 | 0.97 | 1 | |
| rs4341581 | 1.000 | 0.040 | 12 | 71941293 | intron variant | G/T | snv | 0.97 | 1 | ||
| rs3759914 | 1.000 | 0.040 | 15 | 92393214 | upstream gene variant | C/T | snv | 0.97 | 1 | ||
| rs1468271 | 1.000 | 0.040 | 7 | 24287362 | intron variant | C/T | snv | 0.97 | 2 | ||
| rs3759916 | 1.000 | 0.040 | 15 | 92392939 | upstream gene variant | C/T | snv | 0.97 | 1 |