Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs745518585 | 1.000 | 3 | 50348775 | missense variant | G/T | snv | 2.8E-05 | 1.4E-05 | 1 | ||
rs886037963 | 1.000 | 3 | 50350001 | stop gained | G/A | snv | 1 | ||||
rs886037965 | 1.000 | 3 | 50349690 | missense variant | A/G | snv | 1 | ||||
rs886037966 | 1.000 | 3 | 50350584 | frameshift variant | GA/- | del | 1 | ||||
rs886037964 | 1.000 | 3 | 50348173 | stop gained | G/A | snv | 1 | ||||
rs149128231 | 1.000 | 3 | 50348728 | missense variant | C/G | snv | 8.0E-05 | 1.3E-04 | 1 | ||
rs771373457 | 1.000 | 9 | 35808833 | missense variant | G/A;T | snv | 4.0E-06; 1.2E-05 | 1 |