| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2070874 | 0.672 | 0.560 | 5 | 132674018 | 5 prime UTR variant | C/T | snv | 0.28 | 0.28 | 27 | |
| rs2107538 | 0.763 | 0.360 | 17 | 35880776 | 5 prime UTR variant | C/T | snv | 0.27 | 11 | ||
| rs2280789 | 0.925 | 0.080 | 17 | 35879999 | intron variant | A/G | snv | 0.16 | 3 | ||
| rs1043673 | 19 | 55000864 | missense variant | C/A | snv | 0.37 | 0.39 | 2 | |||
| rs1650232 | 1.000 | 0.040 | 10 | 79559511 | splice region variant | C/A;T | snv | 3.6E-03; 0.71 | 2 | ||
| rs12930749 | 16 | 27716458 | non coding transcript exon variant | A/G | snv | 0.23 | 1 |