Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750875 | 0.742 | 0.280 | 2 | 47475171 | missense variant | G/A;C | snv | 1.6E-05 | 15 | ||
rs63750217 | 0.807 | 0.240 | 3 | 37048955 | missense variant | G/A;C | snv | 10 | |||
rs63749795 | 0.807 | 0.240 | 3 | 37028833 | stop gained | C/T | snv | 8 | |||
rs63751108 | 0.827 | 0.240 | 2 | 47429881 | stop gained | C/T | snv | 7 | |||
rs267607720 | 0.851 | 0.240 | 3 | 37000952 | splice region variant | C/G;T | snv | 6 | |||
rs267607768 | 0.851 | 0.240 | 3 | 37011867 | splice region variant | G/A;C | snv | 6 | |||
rs267607871 | 0.851 | 0.240 | 3 | 37048515 | splice acceptor variant | A/G | snv | 4.0E-06 | 6 | ||
rs267607940 | 0.851 | 0.240 | 2 | 47416430 | splice donor variant | G/A;T | snv | 6 | |||
rs63749849 | 0.851 | 0.240 | 2 | 47429812 | stop gained | C/T | snv | 6 | |||
rs63750508 | 0.851 | 0.240 | 2 | 47475126 | stop gained | C/G;T | snv | 6 | |||
rs63750540 | 0.851 | 0.240 | 3 | 37025979 | stop gained | A/T | snv | 6 | |||
rs63750610 | 0.851 | 0.240 | 3 | 37048563 | missense variant | C/G;T | snv | 6 | |||
rs63750636 | 0.851 | 0.240 | 2 | 47476492 | stop gained | C/T | snv | 7.0E-06 | 6 | ||
rs63751275 | 0.851 | 0.240 | 3 | 37048973 | missense variant | C/A;G;T | snv | 1.2E-05; 2.0E-05 | 6 | ||
rs587779075 | 0.882 | 0.200 | 2 | 47429830 | stop gained | C/T | snv | 5 | |||
rs1553647894 | 0.882 | 0.200 | 3 | 37020309 | splice acceptor variant | G/A;C | snv | 4 | |||
rs63750047 | 0.925 | 0.200 | 2 | 47475066 | stop gained | C/T | snv | 4 |