Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104894094 | 0.763 | 0.200 | 9 | 21971058 | missense variant | C/A;G;T | snv | 8.5E-06; 4.3E-06 | 12 | ||
| rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 8 | ||
| rs104894098 | 0.851 | 0.200 | 9 | 21970982 | missense variant | A/T | snv | 5 | |||
| rs104894099 | 0.851 | 0.200 | 9 | 21971183 | missense variant | A/C;T | snv | 4.6E-06 | 5 | ||
| rs1800586 | 0.851 | 0.240 | 9 | 21974861 | 5 prime UTR variant | C/A;G;T | snv | 4.3E-05; 6.1E-05; 8.7E-06 | 5 | ||
| rs749714198 | 0.882 | 0.200 | 9 | 21971100 | missense variant | G/A | snv | 8.6E-06 | 7.0E-06 | 4 | |
| rs587776716 | 0.925 | 0.160 | 9 | 21971115 | frameshift variant | CGGGTCGGGTGAGAGTGGC/- | del | 2 |