Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs74315321 | 0.882 | 0.080 | 1 | 34784887 | missense variant | G/A;C | snv | 1.2E-05 | 5 | ||
rs587777598 | 0.851 | 0.200 | 6 | 79921662 | missense variant | C/G;T | snv | 4 | |||
rs74315316 | 0.925 | 0.080 | 1 | 34784797 | missense variant | G/A | snv | 4 | |||
rs74315318 | 0.925 | 0.200 | 1 | 34785309 | missense variant | G/A | snv | 6.4E-04 | 1.8E-04 | 3 | |
rs28937583 | 0.925 | 0.080 | 1 | 34784863 | missense variant | T/C | snv | 3 | |||
rs74315315 | 0.925 | 0.080 | 1 | 34784796 | missense variant | G/A;C | snv | 3.2E-05 | 2 | ||
rs80358211 | 0.925 | 0.080 | 1 | 34761289 | missense variant | G/A | snv | 2 | |||
rs148182439 | 1.000 | 0.080 | 1 | 34761640 | stop gained | G/A | snv | 2.3E-04 | 9.1E-05 | 1 |