Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201743423
MAX
1.000 0.040 14 65102315 missense variant C/A snv 8.9E-05 7.0E-05 1
rs80338844 0.776 0.280 11 112088939 missense variant C/T snv 2.0E-05 1.4E-05 2
rs80338845 0.807 0.240 11 112088971 missense variant G/T snv 7.0E-06 2
rs104894302 0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 1
rs104894304 0.827 0.240 11 112094831 missense variant A/G snv 1
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 3
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 3
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 3
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 3
rs377767405
RET
0.827 0.120 10 43114489 missense variant G/A;C;T snv 2
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 1
rs377767430
RET
0.882 0.080 10 43120192 missense variant A/C;G snv 1
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 1
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 1
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 1
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 1
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs36119840 0.807 0.280 5 37816010 missense variant G/A snv 2.3E-03 2.7E-03 3
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 3
rs1553619948
VHL
0.882 0.200 3 10146528 missense variant T/C snv 2
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 2