Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 3
rs104893830
VHL
0.925 0.160 3 10146561 missense variant G/C;T snv 2
rs1553619948
VHL
0.882 0.200 3 10146528 missense variant T/C snv 2
rs28940298
VHL
0.776 0.280 3 10149921 missense variant C/T snv 2.1E-04 1.0E-04 2
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 2
rs5030807
VHL
0.851 0.320 3 10142113 missense variant T/A;C snv 2
rs5030808
VHL
0.882 0.200 3 10142124 missense variant G/A;C;T snv 4.5E-06 2
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 2
rs5030820
VHL
0.827 0.280 3 10149822 missense variant C/G;T snv 8.0E-06 2
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 2
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 2
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 1
rs104893826
VHL
0.882 0.200 3 10142038 missense variant G/A;C snv 1
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 1
rs1553619431
VHL
0.925 0.160 3 10142109 missense variant T/A;C snv 1
rs28940300
VHL
1.000 0.040 3 10149897 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs28940301
VHL
0.925 0.040 3 10149894 missense variant C/G snv 1
rs397516440
VHL
0.851 0.280 3 10142166 missense variant C/G;T snv 4.5E-06 1
rs5030804
VHL
0.925 0.160 3 10142080 missense variant A/C;G;T snv 1
rs5030818
VHL
0.882 0.280 3 10149804 stop gained C/G;T snv 1
rs5030822
VHL
0.925 0.160 3 10149856 missense variant T/A;C;G snv 1
rs5030830
VHL
0.925 0.160 3 10146526 missense variant T/C;G snv 1
rs5030832
VHL
0.925 0.160 3 10146535 missense variant A/G snv 1
rs730882034
VHL
0.925 0.160 3 10142104 missense variant C/G;T snv 1
rs794726890
VHL
0.925 0.160 3 10142092 missense variant G/C;T snv 1