| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10214237 | 1.000 | 0.120 | 5 | 35883632 | downstream gene variant | T/C | snv | 0.21 | 1 | ||
| rs10738626 | 1.000 | 0.120 | 9 | 22373458 | intergenic variant | C/G;T | snv | 1 | |||
| rs10888499 | 1.000 | 0.120 | 1 | 152560266 | intergenic variant | C/A;T | snv | 1 | |||
| rs11205006 | 1.000 | 0.120 | 1 | 152467700 | intergenic variant | A/T | snv | 0.72 | 1 | ||
| rs112111458 | 0.925 | 0.120 | 2 | 70872975 | intergenic variant | A/G | snv | 0.16 | 1 | ||
| rs12144049 | 1.000 | 0.120 | 1 | 152468434 | intergenic variant | C/G;T | snv | 1 | |||
| rs12634229 | 0.882 | 0.120 | 3 | 112657461 | intergenic variant | T/C | snv | 0.15 | 1 | ||
| rs13132933 | 0.925 | 0.200 | 4 | 122089432 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
| rs1444418 | 1.000 | 0.120 | 10 | 62800710 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs16999165 | 1.000 | 0.120 | 20 | 54190682 | intergenic variant | A/G | snv | 5.5E-02 | 1 | ||
| rs17389644 | 0.925 | 0.120 | 4 | 122576542 | intergenic variant | G/A;T | snv | 1 | |||
| rs2164983 | 0.925 | 0.120 | 19 | 8679120 | downstream gene variant | C/A;G | snv | 0.19 | 1 | ||
| rs2212434 | 1.000 | 0.120 | 11 | 76570549 | intergenic variant | C/T | snv | 0.39 | 1 | ||
| rs2918307 | 1.000 | 0.120 | 19 | 8679458 | downstream gene variant | A/G;T | snv | 0.19 | 1 | ||
| rs471144 | 1.000 | 0.120 | 1 | 152481779 | intergenic variant | T/G | snv | 8.0E-02 | 1 | ||
| rs4722404 | 0.851 | 0.120 | 7 | 3089155 | intron variant | T/C | snv | 0.40 | 1 | ||
| rs593982 | 1.000 | 0.120 | 11 | 65745636 | upstream gene variant | T/A;C | snv | 1 | |||
| rs61813875 | 1.000 | 0.120 | 1 | 152564174 | downstream gene variant | C/G | snv | 1.6E-02 | 1 | ||
| rs6419573 | 1.000 | 0.120 | 2 | 102410643 | upstream gene variant | T/C | snv | 0.78 | 1 | ||
| rs6473227 | 0.925 | 0.120 | 8 | 80373657 | intron variant | C/A | snv | 0.54 | 1 | ||
| rs6602364 | 1.000 | 0.120 | 10 | 5996890 | regulatory region variant | G/C | snv | 0.50 | 1 | ||
| rs6661961 | 1.000 | 0.120 | 1 | 152469813 | intergenic variant | T/A;C | snv | 1 | |||
| rs7000782 | 1.000 | 0.120 | 8 | 80395915 | intron variant | T/A | snv | 0.54 | 1 | ||
| rs7127307 | 1.000 | 0.120 | 11 | 128317488 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
| rs878860 | 0.882 | 0.120 | 11 | 7946812 | intergenic variant | C/T | snv | 0.35 | 1 |