| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10276303 | 1.000 | 0.120 | 7 | 3279026 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs7291412 | 1.000 | 0.120 | 22 | 46063252 | intron variant | G/T | snv | 0.36 | 1 | ||
| rs1042704 | 1.000 | 0.120 | 14 | 22843385 | missense variant | G/A;C | snv | 0.16 | 1 | ||
| rs1509406 | 1.000 | 0.120 | 15 | 55937562 | intron variant | A/G | snv | 0.30 | 1 | ||
| rs9951109 | 1.000 | 0.120 | 18 | 9762936 | intron variant | T/A;C | snv | 1 | |||
| rs2598107 | 1.000 | 0.120 | 7 | 37933412 | intron variant | C/T | snv | 0.34 | 2 | ||
| rs4730775 | 0.851 | 0.200 | 7 | 117277064 | 3 prime UTR variant | C/T | snv | 0.41 | 1 | ||
| rs394563 | 1.000 | 0.120 | 6 | 149475878 | intron variant | T/C;G | snv | 1 |