Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs867593888 | 0.882 | 0.200 | 22 | 36292059 | missense variant | T/C | snv | 11 | |||
rs80338826 | 0.827 | 0.320 | 22 | 36305985 | missense variant | G/A | snv | 6 | |||
rs80338828 | 0.851 | 0.200 | 22 | 36305975 | missense variant | C/T | snv | 6 | |||
rs80338829 | 0.851 | 0.200 | 22 | 36295069 | missense variant | G/A | snv | 5 | |||
rs121913657 | 0.882 | 0.160 | 22 | 36348950 | missense variant | G/A | snv | 4 | |||
rs80338827 | 0.882 | 0.320 | 22 | 36305984 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
rs80338831 | 0.882 | 0.320 | 22 | 36292060 | missense variant | C/A;G;T | snv | 4 | |||
rs80338830 | 0.925 | 0.160 | 22 | 36295068 | missense variant | C/A | snv | 3 | |||
rs80338834 | 0.925 | 0.160 | 22 | 36284474 | missense variant | C/T | snv | 3 | |||
rs80338835 | 0.925 | 0.200 | 22 | 36282754 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs121913655 | 1.000 | 0.160 | 22 | 36348958 | missense variant | G/A;C | snv | 2.4E-05 | 2 | ||
rs797044804 | 1.000 | 0.160 | 22 | 36291990 | missense variant | T/A | snv | 2 | |||
rs727503284 | 1.000 | 0.160 | 22 | 36289096 | missense variant | C/A | snv | 1 |