| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6102095 | 1.000 | 0.120 | 20 | 40692111 | upstream gene variant | G/A;C | snv | 1 | |||
| rs6519955 | 0.925 | 0.120 | 22 | 46025962 | regulatory region variant | G/T | snv | 0.50 | 1 | ||
| rs7291412 | 1.000 | 0.120 | 22 | 46063252 | intron variant | G/T | snv | 0.36 | 1 | ||
| rs4789939 | 0.925 | 0.120 | 17 | 78885621 | intron variant | T/A;C | snv | 1 | |||
| rs9951109 | 1.000 | 0.120 | 18 | 9762936 | intron variant | T/A;C | snv | 1 | |||
| rs38904 | 1.000 | 0.120 | 7 | 117252792 | intergenic variant | T/C | snv | 0.52 | 2 | ||
| rs17433710 | 1.000 | 0.120 | 1 | 162702221 | intron variant | T/C | snv | 0.12 | 1 | ||
| rs394563 | 1.000 | 0.120 | 6 | 149475878 | intron variant | T/C;G | snv | 1 |