| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs998884 | 1.000 | 0.040 | 2 | 147782283 | intergenic variant | A/G | snv | 0.37 | 1 | ||
| rs9980603 | 0.925 | 0.080 | 21 | 40514656 | intron variant | T/C | snv | 0.40 | 2 | ||
| rs9966951 | 1.000 | 0.040 | 18 | 60108063 | intergenic variant | G/A | snv | 0.34 | 1 | ||
| rs9936170 | 1.000 | 0.040 | 16 | 87477955 | intron variant | A/C;G | snv | 1 | |||
| rs9896243 | 1.000 | 0.040 | 17 | 46748690 | intron variant | C/G | snv | 0.18 | 1 | ||
| rs9870384 | 1.000 | 0.040 | 3 | 84960666 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs9861237 | 1.000 | 0.040 | 3 | 85353319 | intron variant | T/C | snv | 0.39 | 1 | ||
| rs9854869 | 1.000 | 0.040 | 3 | 85371574 | intron variant | C/A | snv | 0.17 | 2 | ||
| rs9837462 | 1.000 | 0.040 | 3 | 85109415 | intron variant | C/A | snv | 0.25 | 1 | ||
| rs9836178 | 1.000 | 0.040 | 3 | 52891387 | intron variant | T/A;C | snv | 1 | |||
| rs9829032 | 0.925 | 0.080 | 3 | 85634450 | intron variant | A/G | snv | 0.41 | 2 | ||
| rs9828595 | 1.000 | 0.040 | 3 | 85843897 | intron variant | T/A;C;G | snv | 1 | |||
| rs9811546 | 1.000 | 0.040 | 3 | 85342522 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs9671386 | 1.000 | 0.040 | 14 | 74684344 | intron variant | G/A | snv | 0.73 | 1 | ||
| rs9470080 | 0.827 | 0.080 | 6 | 35678658 | intron variant | T/A;C | snv | 13 | |||
| rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
| rs9296158 | 0.763 | 0.080 | 6 | 35599305 | intron variant | A/G | snv | 0.65 | 16 | ||
| rs900418273 | 0.807 | 0.120 | 11 | 113393764 | missense variant | A/G | snv | 8 | |||
| rs893924483 | 0.716 | 0.280 | 11 | 27658285 | missense variant | C/A;T | snv | 4.0E-06 | 1.4E-05 | 23 | |
| rs888415 | 1.000 | 0.040 | 14 | 74642492 | regulatory region variant | A/G;T | snv | 1 | |||
| rs876657421 | 0.763 | 0.240 | 21 | 43063074 | coding sequence variant | -/CCCAGCAAAAGCCCCACCTGGATGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG;CCCAGCAAAAGCCCCACCTGGGTGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG | delins | 11 | |||
| rs818219 | 1.000 | 0.040 | 3 | 85325439 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs8067056 | 0.925 | 0.080 | 17 | 46006582 | intron variant | T/C;G | snv | 0.30 | 5 | ||
| rs80533 | 1.000 | 0.040 | 22 | 40689965 | intergenic variant | A/G | snv | 0.81 | 2 | ||
| rs80338903 | 0.701 | 0.360 | 1 | 216247095 | frameshift variant | C/- | del | 7.6E-04 | 5.4E-04 | 25 |