Source: ALL
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 23
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 10
rs28940298
VHL
0.776 0.280 3 10149921 missense variant C/T snv 2.1E-04 1.0E-04 9
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 9
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 8
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 8
rs775387828
NFE2
0.851 0.200 12 54293083 missense variant G/A snv 2.2E-05 7.0E-06 7
rs5030805
VHL
0.790 0.280 3 10142086 missense variant G/A;T snv 7
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 7
rs780178275
VHL
0.851 0.200 3 10146586 missense variant C/T snv 8.0E-06 7
rs1064794272
VHL
0.807 0.240 3 10146566 missense variant C/A snv 6
rs5030820
VHL
0.827 0.280 3 10149822 missense variant C/G;T snv 8.0E-06 6
rs869025667
VHL
0.827 0.200 3 10149916 missense variant T/C snv 6
rs5030807
VHL
0.851 0.320 3 10142113 missense variant T/A;C snv 5
rs5030826
VHL
0.827 0.200 3 10142041 stop gained C/A;G;T snv 5
rs1267580705
EPAS1
0.925 0.240 2 46360680 missense variant G/A snv 4
rs1188254133
VEGFA
0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4
rs104893826
VHL
0.882 0.200 3 10142038 missense variant G/A;C snv 4
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04 4
rs28940297
VHL
0.882 0.240 3 10149811 missense variant T/C;G snv 4
rs397516440
VHL
0.851 0.280 3 10142166 missense variant C/G;T snv 4.5E-06 4
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 4
rs5030818
VHL
0.882 0.280 3 10149804 stop gained C/G;T snv 4
rs5030823
VHL
0.851 0.280 3 10149871 stop gained C/A;G;T snv 4.0E-06 4
rs5030827
VHL
0.882 0.200 3 10142097 missense variant G/A;C;T snv 4.4E-06 4