Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1554691658 | 0.807 | 0.240 | 9 | 95459653 | frameshift variant | C/GGGTCCACAACATCT | delins | 11 | |||
| rs138911275 | 1.000 | 0.120 | 9 | 95458026 | missense variant | G/A | snv | 6.5E-04 | 6.4E-04 | 1 | |
| rs199476091 | 1.000 | 0.120 | 9 | 95479038 | missense variant | C/T | snv | 4.2E-04 | 9.1E-05 | 1 | |
| rs199476093 | 1.000 | 0.120 | 9 | 95459764 | missense variant | A/C | snv | 1 | |||
| rs878853845 | 1.000 | 0.120 | 9 | 95478074 | missense variant | G/A;C | snv | 1 | |||
| rs115556836 | 1.000 | 0.120 | 9 | 95468818 | missense variant | G/A | snv | 1.6E-03 | 6.6E-03 | 1 | |
| rs199476092 | 1.000 | 0.120 | 9 | 95467197 | missense variant | T/C | snv | 9.9E-04 | 3.6E-04 | 1 |