Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2273535 | 0.645 | 0.360 | 20 | 56386485 | missense variant | A/C;T | snv | 0.28 | 38 | ||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs587779157 | 0.827 | 0.240 | 2 | 47408486 | inframe deletion | GAAGTT/- | delins | 6 | |||
rs142155101 | 0.925 | 0.120 | 2 | 214728728 | missense variant | C/T | snv | 1.7E-03 | 1.5E-03 | 3 |