| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4633 | 0.695 | 0.400 | 22 | 19962712 | synonymous variant | C/T | snv | 0.46 | 0.45 | 25 | |
| rs165656 | 0.925 | 0.200 | 22 | 19961340 | intron variant | G/A;C;T | snv | 5 | |||
| rs2070762 | 0.925 | 0.080 | 11 | 2165105 | intron variant | A/G | snv | 0.43 | 5 | ||
| rs1923886 | 13 | 46849156 | intron variant | C/T | snv | 0.64 | 1 | ||||
| rs7330636 | 13 | 46849457 | intron variant | C/T | snv | 0.42 | 1 | ||||
| rs1985242 | 11 | 113977551 | 5 prime UTR variant | A/C;T | snv | 2.6E-05; 0.63 | 1 |