Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs11902171 0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs12881063 1.000 0.080 14 20788017 downstream gene variant G/C snv 7.4E-02 3
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 14
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs771386507 0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs477145 1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2835931 1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs767151455 0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 4
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs16940 0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 21