| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
| rs1137100 | 0.627 | 0.640 | 1 | 65570758 | missense variant | A/G | snv | 0.30 | 0.25 | 39 | |
| rs7799039 | 0.649 | 0.560 | 7 | 128238730 | upstream gene variant | G/A;C | snv | 33 | |||
| rs2854744 | 0.695 | 0.520 | 7 | 45921476 | intron variant | G/T | snv | 0.48 | 20 | ||
| rs121909362 | 0.827 | 0.160 | 5 | 42699919 | missense variant | C/T | snv | 3.9E-03 | 4.1E-03 | 5 | |
| rs60310264 | 0.827 | 0.200 | 1 | 156130693 | missense variant | G/A | snv | 5 | |||
| rs755905735 | 0.851 | 0.160 | 17 | 63917338 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 4 | |
| rs372703574 | 0.851 | 0.160 | 20 | 38146858 | missense variant | G/A | snv | 4.8E-05 | 6.3E-05 | 4 | |
| rs3782415 | 0.925 | 0.280 | 12 | 93573979 | 3 prime UTR variant | T/C | snv | 0.20 | 3 | ||
| rs373184101 | 0.925 | 0.160 | 17 | 63917365 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs6873545 | 0.925 | 0.200 | 5 | 42631162 | intron variant | T/C | snv | 0.31 | 2 | ||
| rs12515480 | 1.000 | 0.160 | 5 | 42464332 | intron variant | C/T | snv | 1.6E-02 | 1 | ||
| rs775145092 | 1.000 | 0.160 | X | 137031083 | missense variant | C/G | snv | 1.6E-05 | 1 | ||
| rs2291340 | 1.000 | 0.160 | 15 | 48255779 | intron variant | T/C;G | snv | 0.27 | 0.36 | 1 |