Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs60682848 | 0.790 | 0.200 | 1 | 156134838 | stop gained | C/T | snv | 7.0E-06 | 11 | ||
rs587777606 | 0.851 | 0.160 | 11 | 62691300 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs137852975 | 0.851 | 0.240 | 11 | 62692671 | stop gained | C/A | snv | 2.0E-05 | 1.4E-05 | 5 | |
rs60458016 | 0.827 | 0.120 | 1 | 156136036 | stop gained | G/A;T | snv | 5 | |||
rs56816490 | 0.925 | 0.120 | 1 | 156135913 | stop gained | G/A;T | snv | 4 | |||
rs267607554 | 1.000 | 0.080 | 1 | 156135925 | stop gained | C/T | snv | 3 | |||
rs267607573 | 1.000 | 0.080 | 1 | 156134865 | stop gained | C/T | snv | 2 | |||
rs267607618 | 1.000 | 0.080 | 1 | 156136350 | stop gained | C/T | snv | 2 | |||
rs1060502211 | 1.000 | 0.080 | 1 | 156135952 | stop gained | G/A;T | snv | 1 | |||
rs1553264593 | 1.000 | 0.080 | 1 | 156130651 | stop gained | C/T | snv | 1 | |||
rs1553265165 | 1.000 | 0.080 | 1 | 156134481 | stop gained | C/T | snv | 1 | |||
rs1553265455 | 1.000 | 0.080 | 1 | 156135253 | stop gained | C/T | snv | 1 | |||
rs1557539119 | 1.000 | 0.080 | 1 | 12011542 | stop gained | C/T | snv | 1 | |||
rs1558115754 | 1.000 | 0.080 | 1 | 156114922 | stop gained | G/T | snv | 1 | |||
rs267607561 | 1.000 | 0.080 | 1 | 156136240 | stop gained | C/A;T | snv | 1.2E-05 | 1.4E-05 | 1 | |
rs267607617 | 1.000 | 0.080 | 1 | 156136027 | stop gained | C/G;T | snv | 4.0E-06 | 1 | ||
rs267607623 | 1.000 | 0.080 | 1 | 156136021 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
rs863224968 | 1.000 | 0.080 | 1 | 12011547 | stop gained | C/A;G;T | snv | 1 | |||
rs878855234 | 1.000 | 0.080 | 1 | 156135304 | stop gained | C/T | snv | 1 | |||
rs879254210 | 1.000 | 0.080 | 1 | 11998873 | stop gained | C/G;T | snv | 1 | |||
rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 29 | |||
rs119103263 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 19 | |||
rs386134243 | 0.708 | 0.360 | 1 | 156135967 | missense variant | C/A;T | snv | 4.0E-06 | 16 | ||
rs137852973 | 0.752 | 0.200 | 11 | 62702493 | missense variant | G/A;C | snv | 7.0E-06 | 13 | ||
rs61672878 | 0.776 | 0.200 | 1 | 156136094 | missense variant | G/A;T | snv | 11 |