Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs752298579 | 0.701 | 0.480 | 22 | 20061538 | missense variant | G/A | snv | 1.4E-04 | 7.0E-06 | 48 | |
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs367814475 | 0.925 | 0.080 | 15 | 40415482 | missense variant | G/C;T | snv | 8.0E-06; 4.0E-06 | 9 | ||
rs121912594 | 0.882 | 0.160 | 2 | 210675762 | missense variant | A/C | snv | 7 | |||
rs121909731 | 0.851 | 0.120 | 10 | 87057692 | missense variant | G/A;C | snv | 4.0E-06 | 7 | ||
rs1555975756 | 1.000 | 0.120 | X | 38401693 | intron variant | G/A | snv | 4 | |||
rs367543005 | 1.000 | 0.120 | 7 | 66089693 | stop gained | C/T | snv | 2 | |||
rs72554356 | 1.000 | 0.120 | X | 38381417 | missense variant | C/T | snv | 1.1E-05 | 2 |