| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13178127 | 1.000 | 0.120 | 5 | 83293613 | intron variant | A/G | snv | 3.3E-02 | 1 | ||
| rs1320767909 | 1.000 | 0.120 | 21 | 45531982 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
| rs1335035506 | 1.000 | 0.120 | 17 | 18340207 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs1447708158 | 1.000 | 0.120 | 3 | 12604160 | synonymous variant | C/T | snv | 7.0E-06 | 1 | ||
| rs146713238 | 1.000 | 0.120 | 5 | 132679861 | missense variant | G/A | snv | 3.2E-05 | 8.4E-05 | 1 | |
| rs148701087 | 1.000 | 0.120 | 17 | 18340762 | missense variant | G/A | snv | 6.4E-04 | 8.8E-04 | 1 | |
| rs150865017 | 1.000 | 0.120 | 3 | 126154627 | missense variant | G/A;T | snv | 1.6E-05; 4.0E-06 | 1 | ||
| rs16994592 | 1.000 | 0.120 | 19 | 6586487 | intron variant | T/C | snv | 9.4E-02 | 1 | ||
| rs17723799 | 1.000 | 0.120 | 5 | 149427514 | non coding transcript exon variant | C/T | snv | 9.9E-02 | 1 | ||
| rs1785882 | 1.000 | 0.120 | 11 | 105052348 | intron variant | A/T | snv | 0.45 | 1 | ||
| rs1790192 | 1.000 | 0.120 | 11 | 118886482 | non coding transcript exon variant | G/A;C | snv | 0.58 | 1 | ||
| rs1800893 | 1.000 | 0.120 | 1 | 206773822 | intron variant | C/T | snv | 0.41 | 1 | ||
| rs1921310 | 1.000 | 0.120 | 2 | 161192690 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs2237060 | 1.000 | 0.120 | 5 | 132635193 | intron variant | T/G | snv | 0.29 | 1 | ||
| rs2582869 | 1.000 | 0.120 | 13 | 108259797 | intron variant | A/G;T | snv | 1 | |||
| rs2637988 | 1.000 | 0.120 | 2 | 113119202 | intron variant | G/A | snv | 0.53 | 1 | ||
| rs2991216 | 1.000 | 0.120 | 9 | 90865745 | intron variant | A/G | snv | 0.21 | 1 | ||
| rs441399 | 1.000 | 0.120 | 15 | 90822992 | regulatory region variant | G/A | snv | 0.50 | 1 | ||
| rs4648022 | 1.000 | 0.120 | 4 | 102575280 | intron variant | C/A;T | snv | 1 | |||
| rs4934436 | 1.000 | 0.120 | 10 | 89023563 | intergenic variant | C/T | snv | 0.60 | 1 | ||
| rs56287471 | 1.000 | 0.120 | 5 | 159323135 | missense variant | C/T | snv | 3.8E-04 | 1.5E-03 | 1 | |
| rs6002551 | 1.000 | 0.120 | 22 | 41942148 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs603097 | 1.000 | 0.120 | 18 | 54226736 | upstream gene variant | G/A | snv | 0.85 | 1 | ||
| rs6736233 | 1.000 | 0.120 | 2 | 201254251 | intron variant | G/C | snv | 0.16 | 1 | ||
| rs754651345 | 1.000 | 0.120 | 5 | 159326751 | missense variant | A/G | snv | 4.0E-06 | 1 |