Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554199368 | 0.827 | 0.160 | 5 | 177256956 | missense variant | C/T | snv | 12 | |||
rs137852671 | 0.790 | 0.160 | 11 | 17394295 | missense variant | C/T | snv | 10 | |||
rs587777732 | 0.763 | 0.240 | 20 | 44406195 | missense variant | C/T | snv | 9 | |||
rs780957825 | 0.827 | 0.160 | 11 | 17387211 | missense variant | G/A;C | snv | 2.0E-05 | 5 | ||
rs121917757 | 0.851 | 0.200 | 11 | 534259 | stop gained | G/A;T | snv | 1.2E-05 | 4 | ||
rs121913236 | 0.882 | 0.160 | 12 | 25245321 | missense variant | G/C;T | snv | 4 |