| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111033563 | 0.776 | 0.240 | 6 | 26092916 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 1 | |
| rs104894226 | 0.658 | 0.560 | 11 | 534285 | missense variant | C/A;G;T | snv | 1 | |||
| rs104894229 | 0.564 | 0.600 | 11 | 534289 | missense variant | C/A;G;T | snv | 1 | |||
| rs104894231 | 0.776 | 0.360 | 11 | 533467 | missense variant | C/G;T | snv | 1 | |||
| rs28933406 | 0.667 | 0.480 | 11 | 533875 | missense variant | G/C;T | snv | 1 | |||
| rs3743930 | 0.611 | 0.720 | 16 | 3254626 | missense variant | C/G;T | snv | 7.1E-02 | 1 | ||
| rs121913250 | 0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv | 1 | |||
| rs562015640 | 0.742 | 0.360 | 10 | 87960957 | stop gained | A/G;T | snv | 1.2E-05 | 1 | ||
| rs121918464 | 0.708 | 0.440 | 12 | 112450406 | missense variant | G/A;C | snv | 1 | |||
| rs74315450 | 0.851 | 0.120 | 21 | 34859485 | missense variant | C/T | snv | 1 | |||
| rs1169288572 | 1.000 | 0.040 | 3 | 47122237 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs754921650 | 1.000 | 0.040 | 3 | 47120446 | missense variant | T/C | snv | 1.2E-05 | 2.1E-05 | 1 | |
| rs387907097 | 0.925 | 0.120 | 20 | 2417445 | missense variant | T/G | snv | 1.5E-04 | 5.6E-05 | 1 | |
| rs1057519985 | 0.724 | 0.360 | 17 | 7673763 | missense variant | T/A;C;G | snv | 1 | |||
| rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 1 | ||
| rs121912651 | 0.605 | 0.680 | 17 | 7674221 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs121913343 | 0.611 | 0.520 | 17 | 7673803 | missense variant | G/A;C;T | snv | 1.2E-05 | 1 | ||
| rs28934576 | 0.554 | 0.600 | 17 | 7673802 | missense variant | C/A;G;T | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs483352695 | 0.882 | 0.200 | 17 | 7674227 | missense variant | T/A;C;G | snv | 1 | |||
| rs587780070 | 0.683 | 0.320 | 17 | 7675077 | missense variant | G/A;C;T | snv | 4.0E-06 | 1 | ||
| rs587781288 | 0.732 | 0.440 | 17 | 7675190 | missense variant | C/A;T | snv | 1 | |||
| rs587782529 | 0.851 | 0.200 | 17 | 7670700 | missense variant | G/A;C | snv | 1 | |||
| rs786201838 | 0.683 | 0.440 | 17 | 7674953 | missense variant | T/A;C;G | snv | 1 | |||
| rs371246226 | 0.827 | 0.160 | 21 | 43094667 | missense variant | T/C;G | snv | 2.4E-05; 2.4E-05 | 1 |