Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913506 | 0.677 | 0.320 | 4 | 54733154 | missense variant | G/A;C;T | snv | 24 | |||
rs1057519710 | 0.695 | 0.280 | 4 | 54733166 | missense variant | G/C;T | snv | 22 | |||
rs28940298 | 0.776 | 0.280 | 3 | 10149921 | missense variant | C/T | snv | 2.1E-04 | 1.0E-04 | 9 | |
rs1555706928 | 0.851 | 0.240 | 18 | 44951954 | missense variant | G/A | snv | 8 | |||
rs104893824 | 0.776 | 0.320 | 3 | 10142181 | missense variant | T/A;C | snv | 8 | |||
rs5030821 | 0.827 | 0.280 | 3 | 10149823 | missense variant | G/A;C;T | snv | 4.0E-06 | 8 | ||
rs755383 | 0.807 | 0.120 | 9 | 863635 | intron variant | C/T | snv | 0.54 | 7 | ||
rs1553632357 | 0.882 | 0.120 | 3 | 41236421 | stop gained | G/T | snv | 5 |