Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1559425925
VHL
1.000 0.120 3 10142079 frameshift variant A/- delins 1
rs5030804
VHL
0.925 0.160 3 10142080 missense variant A/C;G;T snv 3
rs786202787
VHL
1.000 0.120 3 10142085 missense variant A/C;G snv 2
rs1559425951
VHL
1.000 0.120 3 10142085 frameshift variant GTCCGCGCGTCGTGCTGCCCGTA/- delins 1
rs5030805
VHL
0.790 0.280 3 10142086 missense variant G/A;T snv 7
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04 4
rs193922608
VHL
1.000 0.120 3 10142089 missense variant C/A;T snv 4.3E-06; 4.3E-06 2
rs794726890
VHL
0.925 0.160 3 10142092 missense variant G/C;T snv 2
rs5030827
VHL
0.882 0.200 3 10142097 missense variant G/A;C;T snv 4.4E-06 4
rs398123481
VHL
1.000 0.120 3 10142103 missense variant C/G;T snv 2
rs864622545
VHL
0.925 0.160 3 10142103 frameshift variant C/-;CC delins 2
rs730882034
VHL
0.925 0.160 3 10142104 missense variant C/G;T snv 3
rs1553619431
VHL
0.925 0.160 3 10142109 missense variant T/A;C snv 2
rs119103277
VHL
0.925 0.160 3 10142110 stop gained G/A;C snv 3
rs869025622
VHL
0.925 0.160 3 10142111 missense variant G/C;T snv 3
rs5030807
VHL
0.851 0.320 3 10142113 missense variant T/A;C snv 5
rs869025623
VHL
1.000 0.120 3 10142115 frameshift variant A/- delins 1
rs143985153
VHL
1.000 0.120 3 10142116 missense variant A/C;G;T snv 1
rs5030808
VHL
0.882 0.200 3 10142124 missense variant G/A;C;T snv 4.5E-06 3
rs1131690964
VHL
1.000 0.120 3 10142124 frameshift variant G/- delins 2
rs1553619440
VHL
1.000 0.120 3 10142125 missense variant G/A;T snv 1
rs5030829
VHL
1.000 0.120 3 10142127 stop gained G/A;T snv 4.5E-06 2
rs1559426095
VHL
1.000 0.120 3 10142137 frameshift variant TACC/- delins 1
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 10
rs869025624
VHL
1.000 0.120 3 10142139 stop gained -/A delins 1