Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs477145 1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs2835931 1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2269772 0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6
rs2230774 0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs2064863 0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs200081710 1.000 0.120 4 121154648 missense variant T/C snv 7.0E-06 3
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs16940 0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 14
rs1490204625 0.925 0.160 5 87268486 missense variant G/A snv 5
rs1458974438 0.807 0.080 19 1206957 missense variant G/A snv 9