| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7775759 | 0.925 | 0.200 | 6 | 31384669 | upstream gene variant | G/A | snv | 0.36 | 6 | ||
| rs6933050 | 0.925 | 0.200 | 6 | 31375855 | non coding transcript exon variant | T/C | snv | 0.22 | 5 | ||
| rs9266409 | 0.925 | 0.200 | 6 | 31368791 | intron variant | T/C | snv | 0.22 | 5 | ||
| rs76481776 | 0.925 | 0.200 | 7 | 129770387 | non coding transcript exon variant | C/G;T | snv | 5.9E-02 | 4 | ||
| rs104894559 | 0.882 | 0.200 | 17 | 60150074 | missense variant | C/T | snv | 2.5E-04 | 1.4E-04 | 3 | |
| rs1805110 | 0.882 | 0.200 | 1 | 91861488 | missense variant | G/A | snv | 0.13 | 0.13 | 3 | |
| rs3818753 | 1.000 | 0.200 | 1 | 64873549 | 3 prime UTR variant | A/G | snv | 1.0E-02 | 3.6E-03 | 3 | |
| rs4073153 | 1.000 | 0.200 | 9 | 136364897 | non coding transcript exon variant | A/G | snv | 0.40 | 3 | ||
| rs104895083 | 0.925 | 0.200 | 16 | 3247166 | missense variant | G/C;T | snv | 4.0E-05; 1.2E-05 | 2 | ||
| rs12119179 | 0.925 | 0.200 | 1 | 67281732 | downstream gene variant | A/C | snv | 0.30 | 2 | ||
| rs2489188 | 0.925 | 0.200 | 1 | 91866932 | intron variant | C/T | snv | 0.65 | 2 | ||
| rs2903908 | 0.925 | 0.200 | 20 | 46065308 | intron variant | T/C | snv | 0.22 | 2 | ||
| rs4936742 | 0.925 | 0.200 | 11 | 122770378 | intron variant | T/C | snv | 0.64 | 2 | ||
| rs76546355 | 0.925 | 0.200 | 6 | 31381371 | downstream gene variant | G/A | snv | 4.8E-02 | 2 | ||
| rs9517723 | 0.925 | 0.200 | 13 | 99432425 | non coding transcript exon variant | T/C | snv | 0.65 | 2 | ||
| rs10236188 | 1.000 | 0.200 | 7 | 150548168 | intergenic variant | T/C | snv | 0.49 | 1 | ||
| rs10256482 | 1.000 | 0.200 | 7 | 150653887 | intergenic variant | T/C | snv | 0.47 | 1 | ||
| rs10277380 | 1.000 | 0.200 | 7 | 150533604 | intergenic variant | T/A;C | snv | 1 | |||
| rs10454134 | 1.000 | 0.200 | 2 | 48420887 | TF binding site variant | G/A | snv | 0.14 | 1 | ||
| rs1057519328 | 1.000 | 0.200 | 16 | 3249592 | missense variant | G/C | snv | 2.1E-05 | 1 | ||
| rs1065407 | 1.000 | 0.200 | 5 | 96776379 | 3 prime UTR variant | T/A;G | snv | 3.3E-05; 0.26 | 1 | ||
| rs111874856 | 1.000 | 0.200 | 18 | 21028924 | missense variant | C/T | snv | 1 | |||
| rs112108028 | 1.000 | 0.200 | 18 | 20959861 | missense variant | G/A | snv | 1 | |||
| rs112130712 | 1.000 | 0.200 | 18 | 20967783 | missense variant | T/C | snv | 1 | |||
| rs11574944 | 1.000 | 0.200 | 16 | 30498669 | intron variant | C/T | snv | 0.25 | 1 |