| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3775948 | 0.882 | 0.160 | 4 | 9993558 | intron variant | G/A;C | snv | 4 | |||
| rs55951658 | 0.827 | 0.200 | 7 | 99770202 | missense variant | T/A;C | snv | 4.1E-04 | 9.8E-05 | 7 | |
| rs792837 | 1.000 | 0.080 | 3 | 99758338 | intron variant | C/T | snv | 0.51 | 1 | ||
| rs754203 | 0.807 | 0.200 | 14 | 99691630 | non coding transcript exon variant | A/G | snv | 0.27 | 6 | ||
| rs6584273 | 1.000 | 0.080 | 10 | 99379424 | intron variant | G/A | snv | 9.4E-02 | 1 | ||
| rs113816795 | 1.000 | 0.080 | 5 | 99159794 | intergenic variant | T/C | snv | 8.1E-03 | 2 | ||
| rs531564 | 0.672 | 0.480 | 8 | 9903189 | non coding transcript exon variant | G/C | snv | 0.14 | 27 | ||
| rs772820424 | 1.000 | 0.080 | 15 | 98891613 | missense variant | G/A | snv | 5.0E-05 | 2.1E-05 | 1 | |
| rs78761021 | 1.000 | 0.080 | 17 | 9877070 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs9285630 | 1.000 | 0.080 | 1 | 98677991 | intron variant | G/A;C;T | snv | 1 | |||
| rs3739670 | 0.925 | 0.120 | 9 | 98056910 | missense variant | C/G;T | snv | 4.2E-06; 0.27 | 2 | ||
| rs234146 | 1.000 | 0.080 | 14 | 97688175 | intron variant | T/C | snv | 0.85 | 1 | ||
| rs1466100 | 1.000 | 0.080 | 2 | 97655376 | downstream gene variant | T/A;G | snv | 1 | |||
| rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
| rs2072668 | 0.732 | 0.280 | 3 | 9756456 | intron variant | C/G | snv | 0.28 | 0.24 | 14 | |
| rs1801126 | 1.000 | 0.080 | 3 | 9750269 | 5 prime UTR variant | G/T | snv | 4.4E-03 | 2.3E-03 | 1 | |
| rs1801129 | 1.000 | 0.080 | 3 | 9750264 | 5 prime UTR variant | A/G | snv | 1.2E-03 | 4.5E-04 | 1 | |
| rs56387615 | 1.000 | 0.080 | 3 | 9750234 | 5 prime UTR variant | G/A;C | snv | 1 | |||
| rs750392184 | 0.882 | 0.160 | 1 | 9724850 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs1799904 | 1.000 | 0.080 | 5 | 96429259 | missense variant | C/A;T | snv | 4.0E-06; 2.1E-03 | 2 | ||
| rs3811951 | 0.925 | 0.120 | 5 | 96426773 | intron variant | A/G | snv | 0.28 | 2 | ||
| rs6234 | 0.851 | 0.160 | 5 | 96393270 | missense variant | G/C | snv | 0.27 | 0.24 | 8 | |
| rs12050217 | 0.827 | 0.160 | 14 | 96262416 | intron variant | A/G | snv | 0.21 | 6 | ||
| rs79890196 | 1.000 | 0.080 | 15 | 95945146 | intergenic variant | G/A;C;T | snv | 1 | |||
| rs10247649 | 0.925 | 0.080 | 7 | 95586935 | non coding transcript exon variant | A/G | snv | 0.43 | 2 |