Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882020
VHL
0.925 0.160 3 10149798 frameshift variant A/-;AA delins 2
rs1553619461
VHL
1.000 0.120 3 10142160 missense variant A/C snv 1
rs869025643
VHL
1.000 0.120 3 10146547 missense variant A/C snv 1
rs786202787
VHL
1.000 0.120 3 10142085 missense variant A/C;G snv 2
rs864321643
VHL
0.925 0.160 3 10142140 missense variant A/C;G snv 2
rs1347416980
VHL
1.000 0.120 3 10146568 missense variant A/C;G snv 4.0E-06 1
rs5030812
VHL
1.000 0.120 3 10146517 missense variant A/C;G snv 1
rs869025621
VHL
0.882 0.240 3 10142079 missense variant A/C;G;T snv 4
rs5030804
VHL
0.925 0.160 3 10142080 missense variant A/C;G;T snv 3
rs143985153
VHL
1.000 0.120 3 10142116 missense variant A/C;G;T snv 1
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 4
rs869025648
VHL
0.851 0.240 3 10146587 synonymous variant A/G snv 4
rs1271401320 1.000 0.120 9 21440749 missense variant A/G snv 3
rs267607170
VHL
0.882 0.200 3 10149814 missense variant A/G snv 3
rs1559428091
VHL
0.925 0.160 3 10146543 missense variant A/G snv 2
rs5030832
VHL
0.925 0.160 3 10146535 missense variant A/G snv 2
rs1553619963
VHL
1.000 0.120 3 10146565 missense variant A/G snv 1
rs377715747
VHL
1.000 0.120 3 10149861 missense variant A/G snv 8.0E-06 1.4E-05 1
rs869025637
VHL
1.000 0.120 3 10146512 splice acceptor variant A/G snv 1
rs869025642
VHL
1.000 0.120 3 10146531 missense variant A/G snv 1
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs193922613
VHL
0.925 0.160 3 10149847 missense variant A/G;T snv 3
rs5030816
VHL
0.925 0.160 3 10149785 splice acceptor variant A/G;T snv 3
rs1559426203
VHL
0.925 0.160 3 10142178 missense variant A/G;T snv 2
rs1559430011
VHL
1.000 0.120 3 10149965 stop lost A/G;T snv 1