| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs669260 | 0.851 | 0.080 | 9 | 32503442 | intron variant | T/A;C | snv | 4 | |||
| rs2844482 | 0.882 | 0.200 | 6 | 31571990 | upstream gene variant | C/T | snv | 0.15 | 4 | ||
| rs2660 | 0.851 | 0.160 | 12 | 112919637 | missense variant | G/A | snv | 0.71 | 0.75 | 4 | |
| rs3741981 | 0.882 | 0.120 | 12 | 112911065 | missense variant | G/A;C | snv | 3 | |||
| rs10774670 | 1.000 | 0.040 | 12 | 112904357 | upstream gene variant | A/G | snv | 0.65 | 1 | ||
| rs4787947 | 1.000 | 0.040 | 16 | 27307444 | intergenic variant | G/T | snv | 0.92 | 1 | ||
| rs2064479 | 1.000 | 0.040 | 6 | 33104463 | intron variant | C/T | snv | 0.31 | 1 | ||
| rs2284552 | 1.000 | 0.040 | 21 | 33271777 | intron variant | G/T | snv | 0.22 | 1 | ||
| rs2546893 | 1.000 | 0.040 | 5 | 159328952 | intron variant | G/A | snv | 0.42 | 1 | ||
| rs2857708 | 1.000 | 0.040 | 6 | 31565829 | intergenic variant | C/T | snv | 0.10 | 1 | ||
| rs7801617 | 1.000 | 0.040 | 7 | 22718463 | intron variant | G/A | snv | 0.20 | 1 |