Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs169068 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs121913385 0.763 0.240 9 21971112 missense variant G/A;C snv 9
rs61734659 0.790 0.160 7 142774035 missense variant G/A snv 1.4E-02 8
rs748405415 0.790 0.160 7 142773993 stop gained G/A;T snv 8
rs1064794292 0.882 0.200 9 21974760 missense variant C/T snv 3
rs1399364791 0.882 0.240 12 55967046 missense variant G/A snv 4.0E-06 3
rs200081710 1.000 0.120 4 121154648 missense variant T/C snv 7.0E-06 3
rs764664272 1.000 0.120 16 55484060 missense variant A/G snv 1.2E-05 7.0E-06 2
rs786202134 1.000 0.120 19 1220490 missense variant C/A;G;T snv 2
rs756231248 1.000 0.120 17 28735342 missense variant G/C snv 1
rs1057520013 1.000 0.120 11 8436118 missense variant A/C snv 1
rs1057520011
TTK
1.000 0.120 6 80038006 missense variant G/T snv 1