| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7846314 | 8 | 60738272 | intron variant | A/T | snv | 0.27 | 5 | ||||
| rs35914442 | 8 | 60724328 | intron variant | A/G | snv | 0.17 | 2 | ||||
| rs4449834 | 8 | 60843309 | intron variant | G/T | snv | 0.71 | 2 | ||||
| rs13269361 | 0.925 | 0.040 | 8 | 60694892 | intron variant | A/G | snv | 0.10 | 2 | ||
| rs4738817 | 8 | 60708054 | intron variant | G/A | snv | 0.36 | 1 | ||||
| rs7845701 | 8 | 60711732 | intron variant | T/A;C;G | snv | 1 | |||||
| rs10094382 | 8 | 60860726 | intron variant | C/T | snv | 0.46 | 1 | ||||
| rs13280978 | 8 | 60791496 | intron variant | C/T | snv | 0.52 | 1 | ||||
| rs900504 | 8 | 60739148 | intron variant | G/A | snv | 0.45 | 1 | ||||
| rs4237036 | 8 | 60788498 | intron variant | C/T | snv | 0.52 | 1 | ||||
| rs6994642 | 8 | 60811218 | intron variant | C/T | snv | 0.18 | 1 | ||||
| rs7842389 | 8 | 60772635 | intron variant | C/T | snv | 0.77 | 1 | ||||
| rs13277976 | 8 | 60766479 | intron variant | A/T | snv | 0.77 | 1 | ||||
| rs4289855 | 1.000 | 0.040 | 8 | 60799811 | intron variant | T/C | snv | 0.84 | 1 | ||
| rs10957156 | 8 | 60716842 | intron variant | G/A | snv | 0.77 | 1 |