Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 21
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 21
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 21
rs149617956 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 20
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 18
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 17
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 16
rs34677591 0.742 0.120 11 112086941 missense variant G/A snv 7.5E-03 7.0E-03 12
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 11
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 11
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 10
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 10
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs377767406
RET
0.776 0.120 10 43114491 missense variant G/A;T snv 4.0E-05; 4.0E-06 8
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 8
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 7
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 7
rs5030805
VHL
0.790 0.280 3 10142086 missense variant G/A;T snv 7
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 6
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 6
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 6
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 6