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