| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3816769 | 0.851 | 0.240 | 17 | 42346255 | intron variant | T/A;C | snv | 4 | |||
| rs78645479 | 0.851 | 0.120 | 1 | 63322631 | 5 prime UTR variant | C/G;T | snv | 4 | |||
| rs57348955 | 0.882 | 0.120 | 16 | 31174561 | upstream gene variant | G/A;C | snv | 3 | |||
| rs7537605 | 0.882 | 0.120 | 1 | 107800465 | intron variant | G/A;T | snv | 3 | |||
| rs180223 | 0.925 | 0.120 | 8 | 132888007 | missense variant | T/A;C;G | snv | 8.0E-06; 4.0E-06; 0.58 | 2 | ||
| rs2071403 | 0.925 | 0.120 | 2 | 1413472 | 5 prime UTR variant | A/G;T | snv | 2 | |||
| rs327463 | 0.925 | 0.120 | 14 | 80784911 | missense variant | T/C;G | snv | 0.38; 4.1E-06 | 2 | ||
| rs3753348 | 0.925 | 0.080 | 1 | 1208277 | upstream gene variant | C/G;T | snv | 2 | |||
| rs12507813 | 1.000 | 0.040 | 4 | 165013422 | upstream gene variant | G/A;C;T | snv | 1 | |||
| rs165501 | 1.000 | 0.040 | 3 | 10167559 | intron variant | T/A;C | snv | 1 | |||
| rs121434569 | 0.581 | 0.520 | 7 | 55181378 | missense variant | C/T | snv | 2.8E-05 | 5.6E-05 | 70 | |
| rs121917864 | 0.645 | 0.520 | 4 | 153704936 | missense variant | C/T | snv | 8.8E-05 | 9.8E-05 | 31 | |
| rs2291282 | 0.882 | 0.120 | 17 | 42346547 | intron variant | T/C | snv | 1.2E-03 | 3.4E-04 | 3 | |
| rs111033243 | 0.827 | 0.400 | 7 | 107689112 | missense variant | T/C | snv | 6.1E-04 | 8.1E-04 | 5 | |
| rs75201096 | 1.000 | 0.040 | 9 | 77483984 | intron variant | T/C | snv | 1.6E-02 | 1 | ||
| rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
| rs2009895 | 1.000 | 0.040 | 15 | 101276024 | intron variant | C/A;T | snv | 3.0E-02 | 1 | ||
| rs9607715 | 1.000 | 0.040 | 22 | 40399790 | intron variant | G/A | snv | 3.4E-02 | 1 | ||
| rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
| rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 87 | |
| rs4684677 | 0.742 | 0.360 | 3 | 10286769 | missense variant | T/A | snv | 0.10 | 6.6E-02 | 13 | |
| rs5742909 | 0.614 | 0.680 | 2 | 203867624 | upstream gene variant | C/T | snv | 6.7E-02 | 40 | ||
| rs3792876 | 0.790 | 0.280 | 5 | 132301616 | intron variant | C/T | snv | 6.9E-02 | 7 | ||
| rs696217 | 0.662 | 0.640 | 3 | 10289773 | missense variant | G/T | snv | 8.8E-02 | 7.1E-02 | 32 | |
| rs1799969 | 0.637 | 0.560 | 19 | 10284116 | missense variant | G/A | snv | 0.11 | 9.3E-02 | 38 |