Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1085307993 | 0.716 | 0.440 | 5 | 161331056 | missense variant | C/T | snv | 53 | |||
rs267606826 | 0.708 | 0.520 | 14 | 28767903 | stop gained | C/A;G;T | snv | 38 | |||
rs146539065 | 0.752 | 0.240 | 4 | 25145092 | synonymous variant | C/T | snv | 2.8E-05 | 4.2E-05 | 34 | |
rs776969714 | 0.752 | 0.240 | 4 | 25145129 | splice acceptor variant | -/C | delins | 4.2E-05 | 34 | ||
rs1563183492 | 0.708 | 0.520 | 7 | 70766248 | missense variant | C/T | snv | 32 | |||
rs752746786 | 0.742 | 0.560 | 1 | 1806503 | missense variant | A/C;G;T | snv | 4.0E-06 | 30 | ||
rs1554389088 | 0.807 | 0.160 | 7 | 44243526 | missense variant | G/A | snv | 27 | |||
rs869312824 | 0.827 | 0.200 | 1 | 1804565 | missense variant | A/G | snv | 14 | |||
rs1556914274 | 0.790 | 0.440 | X | 53537626 | missense variant | G/A | snv | 13 | |||
rs759317757 | 0.807 | 0.280 | 8 | 91078416 | frameshift variant | TTAAC/- | delins | 12 | |||
rs188675529 | 0.827 | 0.240 | 16 | 67842794 | missense variant | C/G;T | snv | 1.6E-03 | 6.0E-04 | 11 | |
rs776679653 | 0.827 | 0.200 | 9 | 86266174 | missense variant | C/T | snv | 4.2E-06 | 11 | ||
rs753242774 | 0.882 | 0.120 | 3 | 47848237 | missense variant | C/A;T | snv | 9 | |||
rs1555696625 | 0.851 | 0.360 | 19 | 13025409 | missense variant | G/A | snv | 7 |