Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554333853 | 0.689 | 0.320 | 7 | 40046006 | missense variant | A/G | snv | 54 | |||
rs61750420 | 0.689 | 0.480 | 7 | 92501562 | missense variant | C/T | snv | 3.2E-04 | 3.5E-04 | 52 | |
rs398124401 | 0.695 | 0.480 | 4 | 55346393 | stop gained | G/A | snv | 1.2E-04 | 2.8E-05 | 26 | |
rs138659167 | 0.807 | 0.320 | 11 | 71435840 | splice acceptor variant | C/A;G | snv | 5.6E-05; 3.9E-03 | 20 | ||
rs1032242817 | 0.807 | 0.320 | 11 | 71441307 | stop gained | C/T | snv | 8.0E-06 | 7.0E-06 | 17 | |
rs75184679 | 0.776 | 0.360 | 13 | 50945445 | missense variant | G/A | snv | 1.4E-03 | 1.4E-03 | 16 | |
rs778139192 | 0.776 | 0.360 | 15 | 89629561 | stop gained | G/A;T | snv | 4.1E-06; 7.3E-05 | 14 | ||
rs758022116 | 0.790 | 0.280 | 20 | 38535152 | missense variant | G/T | snv | 4.0E-06 | 13 | ||
rs1057518934 | 0.851 | 0.240 | 15 | 28211095 | frameshift variant | G/- | delins | 8 | |||
rs1064796460 | 0.790 | 0.400 | 12 | 49185197 | missense variant | C/G;T | snv | 8 | |||
rs1555303073 | 0.851 | 0.120 | 13 | 110176912 | missense variant | C/T | snv | 6 | |||
rs12877501 | 0.925 | 0.160 | 13 | 110512039 | missense variant | G/A;C | snv | 5.0E-04 | 4 | ||
rs869312878 | 0.882 | 0.160 | 7 | 70766130 | frameshift variant | -/C | delins | 3 | |||
rs1057523820 | 1.000 | 0.120 | X | 41553740 | missense variant | G/A | snv | 1 |