Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
rs151344517 | 0.742 | 0.320 | 18 | 12337505 | missense variant | C/T | snv | 31 | |||
rs121434491 | 0.752 | 0.200 | 2 | 55871091 | missense variant | G/A | snv | 15 | |||
rs1057516030 | 0.807 | 0.280 | 21 | 37480785 | stop gained | -/A | delins | 14 | |||
rs768933093 | 0.807 | 0.240 | 12 | 76348214 | missense variant | G/A | snv | 4.8E-05 | 4.9E-05 | 10 | |
rs61755792 | 0.763 | 0.160 | 6 | 42721821 | missense variant | G/A;C | snv | 10 | |||
rs104893620 | 0.851 | 0.120 | 2 | 98395999 | missense variant | C/T | snv | 9.5E-05 | 7.0E-05 | 6 | |
rs1057518767 | 0.851 | 0.120 | 1 | 94098874 | missense variant | A/T | snv | 5 | |||
rs398123339 | 0.851 | 0.120 | 1 | 94113068 | splice acceptor variant | T/C | snv | 4.0E-06 | 5 | ||
rs61750654 | 0.925 | 0.120 | 1 | 94000870 | stop gained | G/A | snv | 2.0E-05 | 7.0E-06 | 5 | |
rs111033578 | 0.827 | 0.200 | 11 | 119339574 | missense variant | G/C | snv | 5 | |||
rs61755787 | 0.882 | 0.120 | 6 | 42721866 | missense variant | C/T | snv | 5 | |||
rs148957473 | 0.827 | 0.160 | 20 | 25077762 | missense variant | T/C;G | snv | 2.7E-03 | 5 | ||
rs61751406 | 0.925 | 0.120 | 1 | 94014622 | missense variant | G/T | snv | 2.0E-05 | 2.8E-05 | 4 | |
rs1463729 | 0.925 | 0.120 | 9 | 124119169 | intergenic variant | C/A;T | snv | 3 | |||
rs1867315 | 0.882 | 0.120 | 15 | 78977393 | intron variant | C/G;T | snv | 3 |