Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs2835931 1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145 1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1179251 0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1052667 0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs2269772 0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6
rs771386507 0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs767151455 0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 4
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 14
rs931127 0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs115160714 0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9
rs746429 0.882 0.120 11 65649963 synonymous variant G/A snv 0.31 0.30 8