Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519389 | 0.695 | 0.400 | 10 | 129957324 | missense variant | C/A;G;T | snv | 46 | |||
rs61752717 | 0.583 | 0.840 | 16 | 3243407 | missense variant | T/A;C | snv | 2.8E-04 | 20 | ||
rs1555582065 | 0.827 | 0.160 | 17 | 44212851 | missense variant | C/T | snv | 13 | |||
rs863225094 | 0.827 | 0.160 | 19 | 52213076 | missense variant | G/A | snv | 10 | |||
rs878853165 | 0.882 | 0.200 | 19 | 12843558 | missense variant | C/T | snv | 6 | |||
rs869312671 | 0.882 | 0.160 | 1 | 11144735 | missense variant | C/T | snv | 5 |