Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
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
rs5030805
VHL
0.790 0.280 3 10142086 missense variant G/A;T 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
rs5030833
VHL
0.925 0.160 3 10146580 missense variant T/C;G 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
rs104893825
VHL
1.000 0.120 3 10149819 missense variant G/T snv 1
rs104893826
VHL
0.882 0.200 3 10142038 missense variant G/A;C snv 1
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04 1
rs1064793878
VHL
1.000 0.120 3 10149874 missense variant T/C snv 1
rs1064794272
VHL
0.807 0.240 3 10146566 missense variant C/A snv 1
rs119103277
VHL
0.925 0.160 3 10142110 stop gained G/A;C snv 1
rs121913346
VHL
0.925 0.240 3 10149796 missense variant T/A;C snv 1
rs1352275281
VHL
1.000 0.120 3 10149815 missense variant G/C;T snv 8.0E-06 1
rs1553619431
VHL
0.925 0.160 3 10142109 missense variant T/A;C snv 1
rs1553619440
VHL
1.000 0.120 3 10142125 missense variant G/A;T snv 1