| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34560261 | 0.882 | 0.040 | 15 | 90191194 | intron variant | C/T | snv | 0.12 | 3 | ||
| rs6428829 | 0.925 | 0.040 | 1 | 119512118 | intron variant | A/G | snv | 0.78 | 2 | ||
| rs10911268 | 1.000 | 0.040 | 1 | 183153583 | intergenic variant | C/A | snv | 0.39 | 1 | ||
| rs1092479 | 1.000 | 0.040 | 2 | 121011861 | intergenic variant | G/C | snv | 0.39 | 1 | ||
| rs11118336 | 1.000 | 0.040 | 1 | 219547941 | intergenic variant | C/T | snv | 0.51 | 1 | ||
| rs1159268 | 1.000 | 0.040 | 1 | 218671564 | regulatory region variant | G/A | snv | 0.32 | 1 | ||
| rs1256580 | 1.000 | 0.040 | 1 | 219026038 | intron variant | G/C | snv | 0.29 | 1 | ||
| rs144991069 | 1.000 | 0.040 | 11 | 65060236 | upstream gene variant | T/A | snv | 6.8E-03 | 1 | ||
| rs1533326 | 1.000 | 0.040 | 15 | 90211722 | intron variant | A/G | snv | 0.39 | 1 | ||
| rs158639 | 1.000 | 0.040 | 5 | 56315883 | intron variant | G/A | snv | 0.33 | 1 | ||
| rs17651189 | 1.000 | 0.040 | 22 | 24448915 | intron variant | T/C | snv | 2.9E-02 | 1 | ||
| rs2242095 | 1.000 | 0.040 | 8 | 143596704 | 5 prime UTR variant | C/T | snv | 0.15 | 1 | ||
| rs2727365 | 1.000 | 0.040 | 11 | 13089937 | intron variant | G/A;T | snv | 1 | |||
| rs28360612 | 1.000 | 0.040 | 22 | 24487250 | intron variant | T/A | snv | 0.20 | 1 | ||
| rs28405582 | 1.000 | 0.040 | 3 | 23863271 | intron variant | T/C | snv | 4.6E-02 | 1 | ||
| rs28570522 | 1.000 | 0.040 | 8 | 10773058 | intron variant | A/G | snv | 0.66 | 1 | ||
| rs2901000 | 1.000 | 0.040 | 2 | 60274081 | intergenic variant | A/G | snv | 0.62 | 1 | ||
| rs330071 | 1.000 | 0.040 | 8 | 9302385 | intron variant | G/A | snv | 0.25 | 1 | ||
| rs38055 | 1.000 | 0.040 | 5 | 53264814 | intergenic variant | A/G | snv | 0.75 | 1 | ||
| rs4487353 | 1.000 | 0.040 | 4 | 123332634 | intergenic variant | G/A | snv | 0.53 | 1 | ||
| rs478304 | 1.000 | 0.040 | 11 | 65726789 | upstream gene variant | G/T | snv | 0.54 | 1 | ||
| rs61744384 | 1.000 | 0.040 | 11 | 65619907 | synonymous variant | T/A;G | snv | 0.45; 4.1E-06 | 1 | ||
| rs629725 | 1.000 | 0.040 | 5 | 53335237 | TF binding site variant | T/C | snv | 0.74 | 1 | ||
| rs6684868 | 1.000 | 0.040 | 1 | 218674648 | TF binding site variant | G/A | snv | 0.41 | 1 | ||
| rs72966077 | 1.000 | 0.040 | 2 | 218894507 | intron variant | C/T | snv | 3.3E-02 | 1 |