Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5030807
VHL
0.851 0.320 3 10142113 missense variant T/A;C snv 5
rs121913346
VHL
0.925 0.240 3 10149796 missense variant T/A;C snv 3
rs1553619431
VHL
0.925 0.160 3 10142109 missense variant T/A;C snv 2
rs864321642
VHL
0.925 0.160 3 10149832 missense variant T/A;C snv 2
rs1559429824
VHL
1.000 0.120 3 10149886 missense variant T/A;C snv 1
rs193922611
VHL
1.000 0.120 3 10146631 missense variant T/A snv 1
rs398123482
VHL
1.000 0.120 3 10142173 missense variant T/A snv 1
rs869025653
VHL
1.000 0.120 3 10146613 frameshift variant T/-;TT delins 1
rs1559429778
VHL
1.000 0.120 3 10149870 frameshift variant T/- del 1
rs397516442
VHL
1.000 0.120 3 10146579 frameshift variant T/- delins 1
rs869025620
VHL
1.000 0.120 3 10142068 frameshift variant T/- del 1
rs869025627
VHL
1.000 0.120 3 10142156 frameshift variant T/- del 1
rs869025663
VHL
1.000 0.120 3 10149818 frameshift variant GTCCGGAGCCT/- delins 1
rs1559425951
VHL
1.000 0.120 3 10142085 frameshift variant GTCCGCGCGTCGTGCTGCCCGTA/- delins 1
rs1064796408
VHL
0.925 0.160 3 10142023 frameshift variant GGCCCGTGCTGCGC/- delins 2
rs869025647
VHL
1.000 0.120 3 10142036 frameshift variant GCGC/- del 1
rs869025629
VHL
1.000 0.120 3 10142157 splice donor variant GCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAGG/- delins 1
rs869025645
VHL
1.000 0.120 3 10146554 missense variant GC/TT mnv 1
rs869025652
VHL
0.925 0.160 3 10146608 frameshift variant GC/- del 2
rs1553620305
VHL
1.000 0.120 3 10149797 frameshift variant GAA/C delins 1
rs1553620362
VHL
1.000 0.120 3 10149907 frameshift variant GA/- delins 1
rs869025668
VHL
0.882 0.240 3 10149964 stop lost G/T snv 3
rs104893825
VHL
1.000 0.120 3 10149819 missense variant G/T snv 2
rs104893830
VHL
0.925 0.160 3 10146561 missense variant G/C;T snv 3
rs869025622
VHL
0.925 0.160 3 10142111 missense variant G/C;T snv 3