Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 33
rs28936670 0.708 0.280 5 173235011 missense variant G/A snv 3.4E-03 1.1E-02 17
rs387906769 0.807 0.080 8 11708799 missense variant C/T snv 7.3E-05 4.2E-05 7
rs104893904 0.807 0.160 5 173235023 missense variant C/G snv 1.1E-03 7.1E-04 6
rs28939668 0.807 0.200 20 10652533 missense variant C/T snv 6
rs115099192 0.827 0.080 8 11758366 missense variant C/A;G snv 5.1E-04; 6.8E-05 5
rs121908601 0.851 0.080 8 105419192 missense variant A/C;G snv 4.0E-06; 2.7E-03 4
rs187043152 0.851 0.080 8 105801714 missense variant G/A;T snv 3.4E-03; 4.0E-06 4
rs387906816 0.882 0.080 18 22171695 missense variant G/A snv 8.4E-04 1.5E-04 4
rs56208331 0.925 0.080 8 11758419 missense variant G/A;T snv 2.0E-03 4
rs121908603 0.882 0.120 8 105802189 missense variant A/C;G snv 4.9E-04; 4.0E-06 3
rs121918351 0.882 0.240 20 10658611 missense variant C/T snv 3
rs2228638 1.000 0.080 10 33186354 missense variant C/T snv 0.12 9.4E-02 3
rs387906818 0.882 0.120 18 22181516 missense variant C/T snv 3
rs104893902 0.925 0.080 5 173232888 missense variant G/A snv 7.0E-06 2
rs104893905 0.925 0.080 5 173232898 missense variant G/A snv 4.4E-06 2
rs1185861796 1.000 0.080 8 11758339 missense variant C/A snv 8.0E-06 7.0E-06 2
rs145895196 0.925 0.120 20 10641566 missense variant C/A;T snv 1.6E-05; 1.9E-03 2
rs201442000 0.925 0.080 5 173235019 missense variant T/C;G snv 1.3E-04; 4.1E-06 2
rs563655306 0.925 0.080 6 139373371 missense variant T/C snv 3.2E-03 2.0E-03 2
rs769531968 0.925 0.120 20 10643807 missense variant G/A snv 4.0E-06 7.0E-06 2
rs864321699 1.000 0.080 8 11708337 missense variant G/A;C snv 2
rs1057515420 1.000 0.080 7 100819874 missense variant G/A snv 1
rs115875978 1.000 0.080 15 58010691 missense variant C/A;T snv 5.9E-04; 4.0E-06 1
rs121434424 1.000 0.080 19 18869231 missense variant C/A;T snv 2.1E-04 1