Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882031
VHL
1.000 0.120 3 10142039 frameshift variant C/- del 2
rs765978945
VHL
1.000 0.120 3 10142180 missense variant C/G;T snv 4.5E-06 2
rs786202787
VHL
1.000 0.120 3 10142085 missense variant A/C;G snv 2
rs864622109
VHL
1.000 0.120 3 10149878 stop gained C/G;T snv 2
rs869025615
VHL
1.000 0.120 3 10142009 frameshift variant G/-;GG delins 2
rs869025618
VHL
1.000 0.120 3 10142061 missense variant T/C snv 2
rs869025631
VHL
1.000 0.120 3 10142179 missense variant G/A;T snv 2
rs104893830
VHL
0.925 0.160 3 10146561 missense variant G/C;T snv 3
rs119103277
VHL
0.925 0.160 3 10142110 stop gained G/A;C snv 3
rs121913346
VHL
0.925 0.240 3 10149796 missense variant T/A;C snv 3
rs1553619976
VHL
0.925 0.160 3 10146593 frameshift variant -/A delins 3
rs193922613
VHL
0.925 0.160 3 10149847 missense variant A/G;T snv 3
rs5030622
VHL
0.925 0.160 3 10149809 stop gained C/A;G snv 3
rs5030804
VHL
0.925 0.160 3 10142080 missense variant A/C;G;T snv 3
rs5030816
VHL
0.925 0.160 3 10149785 splice acceptor variant A/G;T snv 3
rs5030822
VHL
0.925 0.160 3 10149856 missense variant T/A;C;G snv 3
rs5030830
VHL
0.925 0.160 3 10146526 missense variant T/C;G snv 3
rs5030833
VHL
0.925 0.160 3 10146580 missense variant T/C;G snv 4.0E-06 3
rs730882034
VHL
0.925 0.160 3 10142104 missense variant C/G;T snv 3
rs869025622
VHL
0.925 0.160 3 10142111 missense variant G/C;T snv 3
rs869025655
VHL
0.925 0.160 3 10146625 missense variant T/C;G snv 3
rs104893826
VHL
0.882 0.200 3 10142038 missense variant G/A;C snv 4
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 4
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 4
rs5030818
VHL
0.882 0.280 3 10149804 stop gained C/G;T snv 4