| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs8099917 | 0.581 | 0.600 | 19 | 39252525 | upstream gene variant | T/G | snv | 0.16 | 60 | ||
| rs12980275 | 0.701 | 0.360 | 19 | 39241143 | upstream gene variant | A/G | snv | 0.36 | 23 | ||
| rs1458235863 | 0.925 | 0.160 | 8 | 38412424 | 3 prime UTR variant | G/A | snv | 5.6E-05 | 4 | ||
| rs751918319 | 0.925 | 0.160 | X | 8539692 | missense variant | C/T | snv | 2.2E-05 | 2 | ||
| rs747333248 | 0.925 | 0.160 | 8 | 38418234 | missense variant | C/T | snv | 2.4E-05 | 1.4E-05 | 2 | |
| rs780153672 | 0.925 | 0.160 | 8 | 38428352 | missense variant | G/A | snv | 2.8E-05 | 2.1E-05 | 2 | |
| rs886042254 | 0.925 | 0.160 | 8 | 38428079 | missense variant | A/G | snv | 2 | |||
| rs200895370 | 0.925 | 0.160 | 15 | 74417900 | missense variant | G/A;C | snv | 4.0E-04; 4.0E-06 | 2 | ||
| rs776572648 | 0.925 | 0.160 | 15 | 74411886 | missense variant | C/T | snv | 9.2E-05 | 5.6E-05 | 2 | |
| rs886039523 | 1.000 | 0.080 | 8 | 60741583 | stop gained | C/T | snv | 1 | |||
| rs755580322 | 1.000 | 0.080 | 8 | 38415905 | frameshift variant | -/GTGAAGAT | ins | 1 | |||
| rs775445657 | 1.000 | 0.080 | 8 | 38418280 | missense variant | C/A;T | snv | 8.0E-06 | 1 | ||
| rs778861510 | 1.000 | 0.080 | 8 | 38418337 | missense variant | C/A;T | snv | 2.4E-05 | 1 | ||
| rs147436181 | 1.000 | 0.080 | 7 | 84005396 | missense variant | C/T | snv | 1.4E-02 | 1.2E-02 | 1 | |
| rs1300339524 | 1.000 | 0.080 | 15 | 74410827 | missense variant | T/C | snv | 4.0E-06 | 1 |