Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs199474703 | 0.851 | 0.120 | 3 | 46860702 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
rs104893750 | 0.882 | 0.080 | 3 | 46859529 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 3 | |
rs139794067 | 0.925 | 0.080 | 3 | 46860813 | missense variant | G/A;C;T | snv | 7.2E-05; 1.7E-04 | 3 | ||
rs104893748 | 0.925 | 0.080 | 3 | 46859511 | missense variant | T/C | snv | 2 | |||
rs104893749 | 0.925 | 0.080 | 3 | 46859495 | missense variant | C/A;T | snv | 4.0E-06; 2.4E-05 | 2 | ||
rs193922391 | 1.000 | 0.080 | 3 | 46858413 | missense variant | T/C | snv | 5.6E-05 | 2.8E-05 | 1 | |
rs199474702 | 1.000 | 0.080 | 3 | 46860816 | missense variant | T/C | snv | 1 | |||
rs199474707 | 1.000 | 0.080 | 3 | 46859490 | missense variant | C/A;G;T | snv | 1.2E-05; 4.0E-06; 1.6E-05 | 1 |