| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28416651 | 1.000 | 0.040 | 8 | 105552424 | intron variant | G/A;C | snv | 1 | |||
| rs10093110 | 1.000 | 0.040 | 8 | 105553186 | intron variant | G/A;T | snv | 1 | |||
| rs2288904 | 0.807 | 0.240 | 19 | 10631494 | missense variant | A/G | snv | 0.80 | 0.83 | 2 | |
| rs9797861 | 0.790 | 0.200 | 19 | 10632450 | intron variant | C/A;G;T | snv | 5 | |||
| rs342293 | 0.882 | 0.040 | 7 | 106731773 | intron variant | C/G | snv | 0.42 | 3 | ||
| rs2454899 | 1.000 | 0.040 | 5 | 106929424 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs4753788 | 1.000 | 0.040 | 11 | 107221129 | intergenic variant | A/T | snv | 0.38 | 1 | ||
| rs11042937 | 1.000 | 0.040 | 11 | 10723847 | upstream gene variant | G/T | snv | 0.59 | 1 | ||
| rs3758911 | 1.000 | 0.040 | 11 | 107326914 | missense variant | T/A;C | snv | 1.3E-05; 0.29 | 1 | ||
| rs112370447 | 1.000 | 0.040 | 7 | 107536335 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs2189839 | 1.000 | 0.040 | 7 | 107589581 | intron variant | A/G | snv | 0.72 | 1 | ||
| rs7809950 | 1.000 | 0.040 | 7 | 107597362 | intron variant | T/C | snv | 0.77 | 1 | ||
| rs944172 | 1.000 | 0.040 | 9 | 107755513 | TF binding site variant | C/T | snv | 0.73 | 1 | ||
| rs2140480 | 1.000 | 0.040 | 9 | 107763828 | intergenic variant | T/A;C;G | snv | 1 | |||
| rs9486729 | 1.000 | 0.040 | 6 | 107824597 | upstream gene variant | A/C;G | snv | 1 | |||
| rs3741782 | 1.000 | 0.040 | 12 | 108701361 | intron variant | A/G;T | snv | 0.31; 4.0E-06 | 2 | ||
| rs611917 | 1.000 | 0.040 | 1 | 109272630 | non coding transcript exon variant | A/G | snv | 0.28 | 0.32 | 1 | |
| rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 9 | ||
| rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 9 | ||
| rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
| rs602633 | 0.851 | 0.080 | 1 | 109278889 | downstream gene variant | T/G | snv | 0.63 | 3 | ||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 6 | |||
| rs11617955 | 1.000 | 0.040 | 13 | 110165755 | intron variant | T/A | snv | 9.3E-02 | 1 | ||
| rs12866570 | 1.000 | 0.040 | 13 | 110182619 | intron variant | C/T | snv | 9.6E-02 | 1 | ||
| rs638634 | 1.000 | 0.040 | 13 | 110185206 | intron variant | C/T | snv | 0.27 | 1 |