Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs782058451 | 0.882 | 0.120 | 17 | 41767386 | missense variant | T/C | snv | 2.0E-05 | 3 | ||
rs886037753 | 1.000 | 0.120 | 17 | 41769418 | splice region variant | C/A;T | snv | 4.2E-06; 4.2E-06 | 2 | ||
rs113994177 | 1.000 | 0.120 | 17 | 41757422 | frameshift variant | CA/- | del | 1 | |||
rs1555606936 | 1.000 | 0.120 | 17 | 41771667 | frameshift variant | T/- | del | 1 | |||
rs782440692 | 1.000 | 0.120 | 17 | 41767494 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 1 | |
rs782460555 | 1.000 | 0.120 | 17 | 41771784 | stop gained | G/A;T | snv | 8.0E-06 | 1 | ||
rs797046139 | 1.000 | 0.120 | 17 | 41758753 | stop gained | G/A | snv | 1 |