| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7776725 | 1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 | 2 | ||
| rs917727 | 7 | 121378525 | intron variant | C/A;T | snv | 0.33 | 1 | ||||
| rs2536182 | 7 | 121350783 | intron variant | C/G | snv | 0.52 | 1 | ||||
| rs718766 | 7 | 121385448 | intron variant | T/C | snv | 0.29 | 1 | ||||
| rs529951808 | 7 | 121390854 | intron variant | GGGGGGGGGGGGGGGG/-;G;GG;GGG;GGGG;GGGGG;GGGGGG;GGGGGGG;GGGGGGGG;GGGGGGGGG;GGGGGGGGGG;GGGGGGGGGGG;GGGGGGGGGGGG;GGGGGGGGGGGGG;GGGGGGGGGGGGGG;GGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGGG | delins | 5.8E-02 | 1 | ||||
| rs917726 | 7 | 121378803 | intron variant | A/T | snv | 0.31 | 1 | ||||
| rs2536180 | 7 | 121354619 | intron variant | T/C | snv | 0.55 | 1 | ||||
| rs4727923 | 7 | 121390853 | intron variant | C/G;T | snv | 1 | |||||
| rs4727924 | 7 | 121391825 | intron variant | C/T | snv | 0.53 | 1 | ||||
| rs371847000 | 7 | 121390854 | intron variant | GGGGGGGGGGGGGGGG/-;G;GG;GGG;GGGG;GGGGG;GGGGGG;GGGGGGG;GGGGGGGG;GGGGGGGGG;GGGGGGGGGG;GGGGGGGGGGG;GGGGGGGGGGGG;GGGGGGGGGGGGG;GGGGGGGGGGGGGG;GGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGGG | delins | 5.6E-03 | 1 | ||||
| rs58750532 | 7 | 121390854 | intron variant | GGGGGGGGGGGGGGGG/-;G;GG;GGG;GGGG;GGGGG;GGGGGG;GGGGGGG;GGGGGGGG;GGGGGGGGG;GGGGGGGGGG;GGGGGGGGGGG;GGGGGGGGGGGG;GGGGGGGGGGGGG;GGGGGGGGGGGGGG;GGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGGG | delins | 5.9E-04 | 1 | ||||
| rs3801382 | 7 | 121358223 | intron variant | T/A;G | snv | 1 | |||||
| rs2254595 | 7 | 121367195 | intron variant | T/C | snv | 0.56 | 1 |