Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80356618 | 0.807 | 0.200 | 11 | 17387595 | missense variant | C/A;T | snv | 8 | |||
rs121908332 | 0.882 | 0.240 | 8 | 139618677 | missense variant | C/G;T | snv | 5 | |||
rs193929358 | 0.851 | 0.240 | 11 | 17387091 | missense variant | C/T | snv | 5 | |||
rs398122855 | 0.882 | 0.240 | X | 107642384 | missense variant | G/C | snv | 5 | |||
rs80356611 | 0.790 | 0.240 | 11 | 17387943 | missense variant | C/A;G;T | snv | 4.0E-06 | 10 | ||
rs80356624 | 0.752 | 0.240 | 11 | 17387490 | missense variant | C/A;T | snv | 16 | |||
rs1285524167 | 0.807 | 0.280 | 11 | 17475004 | missense variant | C/T | snv | 8.0E-06 | 8 | ||
rs180177035 | 0.752 | 0.280 | 7 | 140801502 | missense variant | T/C | snv | 35 | |||
rs34767364 | 0.701 | 0.280 | 8 | 89971232 | missense variant | G/A;C | snv | 2.5E-03 | 20 | ||
rs369867819 | 0.851 | 0.320 | 11 | 76659963 | stop gained | G/A;T | snv | 4.0E-06 | 5 | ||
rs80356616 | 0.732 | 0.360 | 11 | 17387917 | missense variant | C/T | snv | 19 | |||
rs373145711 | 0.732 | 0.520 | 20 | 32433408 | stop gained | C/T | snv | 2.0E-05 | 2.8E-05 | 25 | |
rs104894228 | 0.605 | 0.560 | 11 | 534286 | missense variant | C/A;G;T | snv | 48 | |||
rs121909224 | 0.627 | 0.560 | 10 | 87933147 | stop gained | C/G;T | snv | 1.2E-05 | 41 | ||
rs121913105 | 0.653 | 0.600 | 4 | 1806163 | missense variant | A/C;T | snv | 30 |