| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17015014 | 1.000 | 0.120 | 4 | 141807619 | regulatory region variant | G/C | snv | 0.16 | 1 | ||
| rs35964658 | 1.000 | 0.120 | 4 | 141758435 | intergenic variant | A/G | snv | 8.6E-02 | 1 | ||
| rs6140264 | 1.000 | 0.120 | 20 | 7395707 | intergenic variant | G/A | snv | 0.15 | 1 | ||
| rs9901160 | 1.000 | 0.120 | 17 | 18371829 | TF binding site variant | G/A | snv | 0.19 | 1 | ||
| rs3213619 | 1.000 | 0.120 | 7 | 87600877 | 5 prime UTR variant | A/G | snv | 5.2E-02 | 1 | ||
| rs2811709 | 1.000 | 0.120 | 9 | 21980152 | intron variant | A/G | snv | 0.88 | 1 | ||
| rs1360756 | 1.000 | 0.120 | 6 | 130828276 | intron variant | C/T | snv | 0.37 | 1 | ||
| rs9388856 | 1.000 | 0.120 | 6 | 130827723 | intron variant | A/T | snv | 0.37 | 1 | ||
| rs199737785 | 1.000 | 0.120 | 2 | 8778656 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs3776932 | 1.000 | 0.120 | 5 | 109850287 | intron variant | T/G | snv | 0.17 | 1 | ||
| rs11868708 | 1.000 | 0.120 | 17 | 18341299 | non coding transcript exon variant | T/A;C;G | snv | 1 | |||
| rs1804742 | 1.000 | 0.120 | 1 | 236899328 | 3 prime UTR variant | C/T | snv | 0.21 | 1 | ||
| rs2282369 | 1.000 | 0.120 | 1 | 236891499 | intron variant | A/G | snv | 0.68 | 1 | ||
| rs12721593 | 1.000 | 0.120 | 8 | 89981417 | missense variant | G/A | snv | 5.8E-04 | 1.2E-04 | 1 | |
| rs761542345 | 1.000 | 0.120 | 16 | 23684056 | missense variant | A/C | snv | 6.0E-05 | 5.6E-05 | 1 | |
| rs765047496 | 1.000 | 0.120 | 16 | 23684058 | missense variant | C/G | snv | 1.2E-05 | 1 | ||
| rs4813720 | 1.000 | 0.120 | 20 | 4816763 | intron variant | A/G | snv | 0.64 | 1 | ||
| rs1020608187 | 1.000 | 0.120 | 12 | 113398843 | missense variant | C/G | snv | 7.0E-06 | 1 | ||
| rs2273027 | 1.000 | 0.120 | 17 | 18347213 | intron variant | C/T | snv | 0.41 | 1 | ||
| rs10417924 | 1.000 | 0.120 | 19 | 41327262 | intron variant | T/C | snv | 0.86 | 1 | ||
| rs6531666 | 1.000 | 0.120 | 4 | 38830547 | intron variant | T/C | snv | 1 | |||
| rs2853542 | 1.000 | 0.120 | 18 | 657685 | 5 prime UTR variant | G/C;T | snv | 1 | |||
| rs1121404 | 1.000 | 0.120 | 16 | 79055972 | intron variant | T/A;C | snv | 1 | |||
| rs6944602 | 0.925 | 0.120 | 7 | 50406053 | downstream gene variant | G/A;T | snv | 2 | |||
| rs10821938 | 0.925 | 0.120 | 10 | 61965014 | intron variant | A/C | snv | 0.56 | 2 |