| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4053798 | 6 | 85233471 | intergenic variant | A/C | snv | 1.00 | 1 | ||||
| rs387092 | 1.000 | 0.040 | 16 | 83858182 | intergenic variant | G/A | snv | 1.00 | 1 | ||
| rs6975094 | 7 | 133494486 | intron variant | G/A | snv | 1.00 | 1 | ||||
| rs621189 | 1 | 25383919 | intron variant | A/T | snv | 1.00 | 1 | ||||
| rs2958557 | 8 | 19394168 | intron variant | T/C | snv | 1.00 | 1 | ||||
| rs4532315 | 1.000 | 0.080 | 5 | 54768502 | intergenic variant | T/G | snv | 0.99 | 1 | ||
| rs26318 | 0.925 | 0.040 | 5 | 116352208 | intron variant | C/T | snv | 0.99 | 3 | ||
| rs6011570 | 20 | 63059658 | intron variant | A/G | snv | 0.99 | 1 | ||||
| rs2325377 | 1.000 | 0.120 | 13 | 71321166 | intergenic variant | C/T | snv | 0.99 | 1 | ||
| rs4758675 | 12 | 122207191 | missense variant | C/A;G | snv | 1.00 | 0.99 | 1 | |||
| rs7740339 | 6 | 139565505 | intron variant | A/G | snv | 0.99 | 1 | ||||
| rs1809803 | 0.925 | 0.040 | 13 | 43657990 | intron variant | C/T | snv | 0.99 | 2 | ||
| rs6451032 | 0.925 | 0.040 | 5 | 33885168 | intron variant | A/T | snv | 0.99 | 2 | ||
| rs1589933 | 2 | 78251007 | intron variant | G/A | snv | 0.99 | 1 | ||||
| rs614754 | 6 | 160084167 | synonymous variant | C/G | snv | 0.99 | 0.99 | 1 | |||
| rs2962508 | 1.000 | 0.080 | 5 | 146158952 | intron variant | T/C | snv | 0.99 | 1 | ||
| rs2869693 | 1.000 | 0.040 | 20 | 49051608 | intron variant | T/G | snv | 0.99 | 1 | ||
| rs4557697 | 1.000 | 0.080 | 8 | 62931072 | intron variant | G/A | snv | 0.99 | 1 | ||
| rs9972552 | 1.000 | 0.040 | 15 | 34104712 | 3 prime UTR variant | A/C | snv | 0.99 | 2 | ||
| rs10930662 | 0.925 | 0.040 | 2 | 174430873 | downstream gene variant | T/C | snv | 0.99 | 2 | ||
| rs840781 | 1.000 | 0.080 | 2 | 65605243 | intron variant | C/A | snv | 0.99 | 1 | ||
| rs186053156 | 7 | 74579359 | intron variant | C/T | snv | 0.99 | 1 | ||||
| rs6531565 | 4 | 37660910 | intron variant | T/A | snv | 0.99 | 2 | ||||
| rs117804109 | 14 | 106265299 | upstream gene variant | C/T | snv | 0.99 | 1 | ||||
| rs4236746 | 8 | 129687615 | non coding transcript exon variant | A/G | snv | 0.99 | 1 |