Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869025621
VHL
0.882 0.240 3 10142079 missense variant A/C;G;T snv 4
rs869025648
VHL
0.851 0.240 3 10146587 synonymous variant A/G snv 4
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
rs1271401320 1.000 0.120 9 21440749 missense variant A/G snv 3
rs1400537035 0.882 0.200 7 101131931 missense variant C/A;G;T snv 3
rs148935214
RET
0.882 0.240 10 43114546 missense variant C/T snv 3.2E-04 3.8E-04 3
rs1553619948
VHL
0.882 0.200 3 10146528 missense variant T/C snv 3
rs193922613
VHL
0.925 0.160 3 10149847 missense variant A/G;T snv 3
rs267607170
VHL
0.882 0.200 3 10149814 missense variant A/G snv 3
rs397516444
VHL
0.882 0.200 3 10149808 missense variant G/A;T snv 4.0E-06 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
rs5030808
VHL
0.882 0.200 3 10142124 missense variant G/A;C;T snv 4.5E-06 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
rs869025650
VHL
0.882 0.160 3 10146603 stop gained G/A;C;T snv 4.0E-06 3
rs869025655
VHL
0.925 0.160 3 10146625 missense variant T/C;G snv 3
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