| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs545854 | 0.882 | 0.160 | 8 | 10002570 | intron variant | G/C | snv | 0.85 | 4 | ||
| rs2054576 | 0.882 | 0.160 | 4 | 88107623 | intron variant | A/G | snv | 7.8E-02 | 4 | ||
| rs201874364 | 1.000 | 0.040 | 3 | 186065822 | missense variant | C/A;T | snv | 4.0E-06; 7.2E-05 | 4 | ||
| rs11554266 | 1.000 | 0.040 | 20 | 58903791 | splice region variant | C/G;T | snv | 4.0E-06; 2.3E-03 | 4 | ||
| rs2941484 | 0.882 | 0.160 | 8 | 75566533 | 3 prime UTR variant | C/T | snv | 0.52 | 4 | ||
| rs147445322 | 0.882 | 0.120 | 11 | 2847803 | missense variant | G/A;T | snv | 7.2E-05; 5.5E-06 | 4 | ||
| rs2544390 | 0.925 | 0.080 | 2 | 169348336 | intron variant | C/T | snv | 0.45 | 4 | ||
| rs141310123 | 0.925 | 0.120 | 18 | 79411390 | missense variant | C/A;T | snv | 2.1E-04; 4.8E-06 | 4 | ||
| rs505802 | 0.882 | 0.160 | 11 | 64589600 | upstream gene variant | T/C | snv | 0.45 | 4 | ||
| rs202007714 | 1.000 | 0.040 | 3 | 66383098 | missense variant | G/A;C | snv | 1.4E-04; 4.0E-06 | 4 | ||
| rs138551969 | 1.000 | 0.040 | 6 | 43780749 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 4 | |
| rs35258188 | 1.000 | 0.040 | 15 | 53705141 | missense variant | T/G | snv | 3.5E-03 | 1.5E-02 | 4 | |
| rs61754122 | 1.000 | 0.040 | 20 | 54028628 | missense variant | C/A;T | snv | 1.1E-02; 8.0E-06 | 3 | ||
| rs200933617 | 1.000 | 0.040 | 16 | 69647162 | missense variant | G/A | snv | 8.2E-04 | 6.7E-04 | 3 | |
| rs4684846 | 0.882 | 0.080 | 3 | 12297350 | intron variant | A/G | snv | 0.28 | 3 | ||
| rs143231463 | 1.000 | 0.040 | 6 | 7226577 | missense variant | A/G | snv | 1.8E-04 | 2.1E-04 | 3 | |
| rs7903456 | 0.882 | 0.160 | 10 | 87159562 | intron variant | C/T | snv | 0.69 | 3 | ||
| rs11602903 | 0.882 | 0.120 | 11 | 64590769 | 5 prime UTR variant | A/T | snv | 0.51 | 3 | ||
| rs3825016 | 0.882 | 0.160 | 11 | 64591814 | synonymous variant | C/T | snv | 0.57 | 0.51 | 3 | |
| rs475688 | 0.882 | 0.160 | 11 | 64596819 | intron variant | C/T | snv | 0.25 | 3 | ||
| rs893006 | 0.882 | 0.160 | 11 | 64598324 | intron variant | C/A | snv | 0.61 | 3 | ||
| rs151305324 | 1.000 | 0.040 | 5 | 73123606 | missense variant | G/A | snv | 6.8E-05; 8.0E-06 | 9.1E-05 | 3 | |
| rs199897813 | 1.000 | 0.040 | 4 | 88094576 | splice donor variant | C/A;T | snv | 5.2E-05 | 2 | ||
| rs72552713 | 0.925 | 0.040 | 4 | 88131805 | stop gained | G/A | snv | 4.0E-04 | 1.2E-04 | 2 | |
| rs200469773 | 0.925 | 0.120 | 2 | 169237232 | missense variant | C/T | snv | 4.0E-05 | 4.2E-05 | 2 |