| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1024708183 | 0.925 | 0.040 | 19 | 7909761 | missense variant | A/G | snv | 4 | |||
| rs10754833 | 0.851 | 0.040 | 1 | 236021631 | intron variant | T/A;C | snv | 4 | |||
| rs12210050 | 0.807 | 0.040 | 6 | 475489 | non coding transcript exon variant | C/T | snv | 0.11 | 4 | ||
| rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 4 | ||
| rs397507482 | 0.882 | 0.040 | 7 | 140753386 | missense variant | A/C | snv | 3 | |||
| rs749496294 | 0.925 | 0.040 | 20 | 3562435 | missense variant | G/A | snv | 1.2E-05 | 1.4E-05 | 3 | |
| rs766310650 | 1.000 | 0.040 | 6 | 36677906 | 5 prime UTR variant | T/C | snv | 6.2E-05 | 2.1E-05 | 3 | |
| rs1057519805 | 1.000 | 0.040 | 15 | 66436839 | missense variant | T/C | snv | 2 | |||
| rs1057519808 | 1.000 | 0.040 | 19 | 4117543 | missense variant | T/G | snv | 2 | |||
| rs121913368 | 0.925 | 0.040 | 7 | 140753345 | missense variant | AG/GA | mnv | 2 | |||
| rs121913371 | 1.000 | 0.040 | 7 | 140781678 | missense variant | G/A;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs138106763 | 1.000 | 0.040 | 7 | 100857102 | missense variant | A/G | snv | 7.2E-05 | 1.2E-04 | 2 | |
| rs1449409868 | 0.925 | 0.040 | 20 | 23035958 | missense variant | C/A;T | snv | 4.1E-06; 4.1E-06 | 2 | ||
| rs1487774219 | 1.000 | 0.040 | 9 | 22008910 | missense variant | T/C | snv | 8.1E-06 | 2 | ||
| rs2074560 | 0.925 | 0.040 | 21 | 41380411 | intron variant | A/G | snv | 0.43 | 2 | ||
| rs700635 | 0.925 | 0.040 | 2 | 201288502 | 3 prime UTR variant | C/A | snv | 0.72 | 2 | ||
| rs755007339 | 1.000 | 0.040 | 1 | 241098711 | missense variant | G/A;C | snv | 1.2E-05; 4.0E-06 | 2 | ||
| rs762807774 | 1.000 | 0.040 | 1 | 1228495 | frameshift variant | CGCGGCTCCGC/-;CGCGGCTCCGCCGCGGCTCCGC | delins | 7.0E-06 | 2 | ||
| rs765857063 | 1.000 | 0.040 | 3 | 12618634 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs776761577 | 1.000 | 0.040 | 6 | 33179444 | missense variant | C/A;T | snv | 2.9E-05 | 2 | ||
| rs778015444 | 1.000 | 0.040 | 4 | 54274917 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs866551255 | 1.000 | 0.040 | 6 | 36684145 | missense variant | G/A | snv | 2 | |||
| rs1015363 | 1.000 | 0.040 | 20 | 34150529 | intergenic variant | G/A | snv | 0.69 | 1 | ||
| rs10231520 | 1.000 | 0.040 | 7 | 20742471 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs10515789 | 1.000 | 0.040 | 5 | 159079407 | intron variant | T/G | snv | 0.11 | 1 |