Disease: Neoplastic Syndromes, Hereditary
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893825
VHL
1.000 0.120 3 10149819 missense variant G/T snv 2
rs1131690964
VHL
1.000 0.120 3 10142124 frameshift variant G/- delins 2
rs193922608
VHL
1.000 0.120 3 10142089 missense variant C/A;T snv 4.3E-06; 4.3E-06 2
rs193922609
VHL
1.000 0.120 3 10142167 missense variant G/A;C snv 2
rs398123481
VHL
1.000 0.120 3 10142103 missense variant C/G;T snv 2
rs5030802
VHL
1.000 0.120 3 10142055 stop gained G/A;T snv 4.4E-06 2
rs5030829
VHL
1.000 0.120 3 10142127 stop gained G/A;T snv 4.5E-06 2
rs587780077
VHL
1.000 0.120 3 10146618 missense variant G/A;C;T snv 2
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