Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 11
rs942160050 0.882 0.080 1 161356685 missense variant C/A;G;T snv 4.0E-06 3
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 7
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 16
rs55846256
RET
0.882 0.120 10 43114493 missense variant C/A;T snv 4.0E-06; 1.3E-04 4
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 8
rs1416313401 0.827 0.160 8 109578004 missense variant A/G snv 4.1E-06 5
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 21
rs5030827
VHL
0.882 0.200 3 10142097 missense variant G/A;C;T snv 4.4E-06 2
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 6
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 10
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 21
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 8
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 6
rs146646971
RET
0.807 0.120 10 43114598 missense variant G/C;T snv 2.4E-05 5
rs377767402
RET
0.882 0.120 10 43113663 missense variant G/A snv 2.4E-05 2.8E-05 4
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs374918502 0.925 0.080 1 156880056 missense variant C/T snv 6.0E-05 7.6E-06 2
rs142441643 0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04 3
rs34682185
RET
0.851 0.120 10 43106382 missense variant G/A snv 6.3E-04 2.2E-04 4
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 20
rs36119840 0.807 0.280 5 37816010 missense variant G/A snv 2.3E-03 2.7E-03 4
rs34677591 0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs62624461 0.851 0.080 7 97117880 missense variant T/C snv 2.0E-02 1.8E-02 4
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27