| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs78686797 | 1.000 | 0.080 | X | 67545316 | missense variant | T/A | snv | 1.1E-03 | 1 | ||
| rs868669253 | 1.000 | 0.080 | X | 67711405 | missense variant | G/A;T | snv | 1 | |||
| rs1851779 | 1.000 | 0.080 | 2 | 197782384 | intron variant | C/T | snv | 0.19 | 1 | ||
| rs2293255 | 1.000 | 0.080 | 2 | 197756782 | intron variant | T/C | snv | 0.20 | 1 | ||
| rs9889335 | 1.000 | 0.080 | 17 | 71119005 | intron variant | T/G | snv | 0.59 | 1 | ||
| rs16901970 | 1.000 | 0.080 | 8 | 127100470 | intron variant | T/G | snv | 0.13 | 1 | ||
| rs7817677 | 1.000 | 0.080 | 8 | 127113259 | intron variant | A/G | snv | 0.13 | 1 | ||
| rs1447293 | 1.000 | 0.080 | 8 | 127460075 | intron variant | C/T | snv | 0.48 | 1 | ||
| rs921146 | 1.000 | 0.080 | 8 | 127462940 | intron variant | G/C;T | snv | 1 | |||
| rs6008813 | 1.000 | 0.080 | 22 | 46416688 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs16972648 | 1.000 | 0.080 | 15 | 81016085 | intron variant | G/A;C | snv | 1 | |||
| rs121908701 | 1.000 | 0.080 | 22 | 28725027 | missense variant | C/T | snv | 1.4E-04 | 6.3E-05 | 1 | |
| rs143611747 | 1.000 | 0.080 | 22 | 28699893 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06; 4.0E-06; 4.8E-05 | 1 | ||
| rs587780189 | 1.000 | 0.080 | 22 | 28711950 | missense variant | T/A | snv | 8.0E-06 | 8.4E-05 | 1 | |
| rs587780194 | 1.000 | 0.080 | 22 | 28699866 | missense variant | T/A;C | snv | 1.6E-05 | 1 | ||
| rs587781667 | 1.000 | 0.080 | 22 | 28725253 | missense variant | C/G;T | snv | 8.0E-06; 1.6E-05 | 1 | ||
| rs750984976 | 1.000 | 0.080 | 22 | 28699879 | missense variant | T/C;G | snv | 4.0E-06 | 1 | ||
| rs629242 | 1.000 | 0.080 | 4 | 56276871 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs147739031 | 1.000 | 0.080 | 8 | 3389886 | intron variant | A/C;G | snv | 1 | |||
| rs142173175 | 1.000 | 0.080 | 1 | 22906770 | missense variant | T/C | snv | 1.2E-03 | 4.7E-03 | 1 | |
| rs201754821 | 1.000 | 0.080 | 1 | 22784861 | missense variant | G/A | snv | 8.8E-05 | 3.5E-05 | 1 | |
| rs372653137 | 1.000 | 0.080 | 1 | 22910526 | missense variant | A/G | snv | 4.0E-05 | 1.8E-04 | 1 | |
| rs35882952 | 1.000 | 0.080 | 1 | 22863060 | missense variant | G/C;T | snv | 4.0E-06; 1.1E-03 | 1 | ||
| rs140712764 | 1.000 | 0.080 | 6 | 6266621 | missense variant | C/T | snv | 1.0E-04 | 2.4E-04 | 1 | |
| rs73043340 | 1.000 | 0.080 | 3 | 33085480 | intron variant | C/T | snv | 0.29 | 1 |