| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 13 | ||
| rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 8 | |
| rs7536458 | 1 | 118321979 | intergenic variant | T/G | snv | 0.23 | 5 | ||||
| rs1812175 | 4 | 144653692 | intron variant | A/G | snv | 0.79 | 5 | ||||
| rs7970350 | 12 | 65966384 | downstream gene variant | C/T | snv | 0.48 | 4 | ||||
| rs724016 | 1.000 | 0.040 | 3 | 141386728 | 5 prime UTR variant | A/G | snv | 0.52 | 4 | ||
| rs1984119 | 9 | 95606479 | upstream gene variant | T/C | snv | 0.24 | 2 | ||||
| rs2280470 | 15 | 88852395 | intron variant | A/G | snv | 0.68 | 2 | ||||
| rs6470764 | 8 | 129713419 | intron variant | C/G;T | snv | 2 | |||||
| rs12534093 | 7 | 23463355 | intron variant | T/A | snv | 0.18 | 2 | ||||
| rs9385399 | 6 | 126437887 | intron variant | G/T | snv | 0.42 | 1 | ||||
| rs1380294 | 4 | 18022498 | upstream gene variant | C/T | snv | 0.25 | 1 | ||||
| rs592229 | 1.000 | 0.080 | 6 | 31962664 | intron variant | G/A;C;T | snv | 4.0E-06; 4.5E-05; 0.61 | 1 | ||
| rs1567865 | 20 | 49265430 | intron variant | C/T | snv | 0.15 | 1 |