| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4674344 | 1.000 | 2 | 218805152 | intron variant | A/T | snv | 0.53 | 1 | |||
| rs2401514 | 1.000 | 22 | 43998139 | intron variant | T/A | snv | 0.20 | 1 | |||
| rs1010022 | 1.000 | 22 | 43940430 | intron variant | A/G | snv | 0.20 | 1 | |||
| rs11090617 | 1.000 | 22 | 43930820 | intron variant | C/T | snv | 0.18 | 1 | |||
| rs1474745 | 1.000 | 22 | 43953356 | intron variant | T/C | snv | 0.19 | 1 | |||
| rs1883349 | 1.000 | 22 | 43936063 | intron variant | G/A | snv | 0.19 | 1 | |||
| rs1883350 | 1.000 | 22 | 43932163 | intron variant | T/C | snv | 0.35 | 1 | |||
| rs2072905 | 1.000 | 22 | 43937599 | intron variant | C/G;T | snv | 1 | ||||
| rs2073081 | 1.000 | 22 | 43939864 | intron variant | T/C | snv | 0.20 | 1 | |||
| rs2294916 | 1.000 | 22 | 43945042 | intron variant | T/G | snv | 0.20 | 1 | |||
| rs4823179 | 1.000 | 22 | 43945313 | intron variant | T/C | snv | 0.20 | 1 | |||
| rs926633 | 1.000 | 22 | 43941653 | intron variant | G/A | snv | 0.20 | 1 | |||
| rs2228530 | 1.000 | 2 | 28778825 | missense variant | A/C;G | snv | 1 | ||||
| rs2073079 | 1.000 | 22 | 43989714 | intron variant | A/G | snv | 0.21 | 1 | |||
| rs2235777 | 1.000 | 22 | 43982929 | intron variant | C/T | snv | 0.24 | 1 | |||
| rs2235778 | 1.000 | 22 | 43993634 | intron variant | T/C | snv | 0.48 | 1 | |||
| rs2281298 | 1.000 | 22 | 43995354 | intron variant | G/A | snv | 0.21 | 1 | |||
| rs2294922 | 1.000 | 22 | 43983685 | intron variant | G/C | snv | 0.30 | 1 | |||
| rs3788604 | 1.000 | 22 | 43992537 | intron variant | A/G | snv | 0.48 | 1 | |||
| rs3827385 | 1.000 | 22 | 43992937 | intron variant | T/C | snv | 0.21 | 1 | |||
| rs6006468 | 1.000 | 22 | 43987552 | non coding transcript exon variant | G/C | snv | 0.48 | 1 | |||
| rs6006469 | 1.000 | 22 | 43987737 | non coding transcript exon variant | C/G | snv | 0.49 | 1 | |||
| rs6006602 | 1.000 | 22 | 43987520 | non coding transcript exon variant | C/T | snv | 0.48 | 1 | |||
| rs1007863 | 1.000 | 22 | 43999571 | missense variant | T/A;C | snv | 0.44 | 1 | |||
| rs2281292 | 1.000 | 22 | 43999509 | intron variant | A/C | snv | 0.44 | 0.47 | 1 |