Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1556026984 | 0.925 | 0.120 | X | 134475194 | missense variant | G/C | snv | 4 | |||
rs387906725 | 0.882 | 0.160 | X | 134475189 | missense variant | G/A | snv | 3 | |||
rs137852485 | 0.925 | 0.120 | X | 134475358 | missense variant | C/A | snv | 2 | |||
rs137852489 | 0.925 | 0.160 | X | 134486471 | stop gained | C/A;T | snv | 2.4E-05 | 2 | ||
rs137852494 | 0.925 | 0.160 | X | 134475197 | stop gained | C/G;T | snv | 2 | |||
rs137852495 | 0.925 | 0.120 | X | 134475216 | missense variant | T/C | snv | 2 | |||
rs137852497 | 0.925 | 0.200 | X | 134498412 | stop gained | C/A;T | snv | 4.4E-05 | 2 | ||
rs1556030169 | 0.925 | 0.160 | X | 134498683 | frameshift variant | -/T | delins | 2 | |||
rs369065223 | 0.925 | 0.160 | X | 134486514 | stop gained | C/G;T | snv | 5.5E-06 | 2 | ||
rs1135401801 | 1.000 | 0.120 | X | 134473378 | missense variant | G/T | snv | 1 | |||
rs1228634091 | 1.000 | 0.120 | X | 134475225 | missense variant | A/G | snv | 1.1E-05 | 1 | ||
rs137852477 | 1.000 | 0.120 | X | 134490199 | missense variant | T/G | snv | 1 | |||
rs137852478 | 1.000 | 0.120 | X | 134475285 | missense variant | A/T | snv | 1 | |||
rs137852479 | 1.000 | 0.120 | X | 134498677 | missense variant | A/G | snv | 1 | |||
rs137852480 | 1.000 | 0.120 | X | 134473453 | missense variant | T/C | snv | 1 | |||
rs137852481 | 1.000 | 0.120 | X | 134475268 | missense variant | C/A | snv | 1 | |||
rs137852482 | 1.000 | 0.120 | X | 134486475 | missense variant | C/T | snv | 1 | |||
rs137852483 | 1.000 | 0.120 | X | 134490192 | missense variant | T/A | snv | 1 | |||
rs137852484 | 1.000 | 0.120 | X | 134493586 | missense variant | G/T | snv | 1 | |||
rs137852486 | 1.000 | 0.120 | X | 134498670 | missense variant | T/G | snv | 1 | |||
rs137852487 | 1.000 | 0.120 | X | 134475255 | missense variant | G/A | snv | 1 | |||
rs137852488 | 1.000 | 0.120 | X | 134475257 | missense variant | G/C | snv | 1 | |||
rs137852490 | 1.000 | 0.120 | X | 134500030 | missense variant | C/G | snv | 1 | |||
rs137852491 | 1.000 | 0.120 | X | 134473465 | missense variant | G/A | snv | 4.4E-05 | 1 | ||
rs137852492 | 1.000 | 0.120 | X | 134498433 | missense variant | G/T | snv | 1 |