| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894073 | 0.827 | 0.080 | 8 | 11750213 | missense variant | G/A;C;T | snv | 8 | |||
| rs387906769 | 0.807 | 0.080 | 8 | 11708799 | missense variant | C/T | snv | 7.3E-05 | 4.2E-05 | 7 | |
| rs115099192 | 0.827 | 0.080 | 8 | 11758366 | missense variant | C/A;G | snv | 5.1E-04; 6.8E-05 | 5 | ||
| rs146017816 | 1.000 | 8 | 11758471 | missense variant | C/G;T | snv | 7.2E-05; 1.6E-05 | 2 | |||
| rs368489876 | 1.000 | 8 | 11757012 | missense variant | G/A | snv | 4.4E-05 | 2.1E-05 | 2 | ||
| rs387906770 | 1.000 | 8 | 11708439 | splice acceptor variant | C/A;T | snv | 2 | ||||
| rs199922907 | 1.000 | 8 | 11708329 | splice donor variant | C/T | snv | 7.0E-06 | 1 |