Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6656401 | 0.776 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 8 | |||
| rs3818361 | 0.851 | 0.080 | 1 | 207611623 | intron variant | A/G | snv | 0.74 | 6 | ||
| rs1344800847 | 0.925 | 0.120 | 1 | 207569911 | missense variant | G/T | snv | 2 | |||
| rs2296160 | 0.925 | 0.120 | 1 | 207621975 | missense variant | A/G | snv | 0.82 | 0.81 | 2 | |
| rs3738467 | 0.925 | 0.120 | 1 | 207552816 | missense variant | G/T | snv | 1.4E-03 | 2 | ||
| rs12036785 | 1.000 | 0.080 | 1 | 207619564 | intron variant | C/A | snv | 0.47 | 1 | ||
| rs1408077 | 1.000 | 0.080 | 1 | 207630796 | intron variant | A/C | snv | 0.84 | 1 | ||
| rs1408078 | 1.000 | 0.080 | 1 | 207627210 | intron variant | T/C | snv | 0.84 | 1 | ||
| rs2093760 | 1.000 | 0.080 | 1 | 207613483 | intron variant | A/G | snv | 0.74 | 1 | ||
| rs4844609 | 1.000 | 0.080 | 1 | 207609571 | missense variant | A/T | snv | 0.99 | 0.99 | 1 | |
| rs4844610 | 1.000 | 0.080 | 1 | 207629207 | intron variant | A/C | snv | 0.87 | 1 | ||
| rs6701713 | 1.000 | 0.080 | 1 | 207612944 | intron variant | A/G;T | snv | 1 | |||
| rs679515 | 1.000 | 0.080 | 1 | 207577223 | intron variant | T/A;C | snv | 1 |