Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148696809 0.851 0.160 6 28966575 downstream gene variant T/C snv 5.3E-02 4
rs568404 0.851 0.120 10 129233875 regulatory region variant C/A;G;T snv 4
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042711 0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs758244932 0.827 0.120 1 225828842 missense variant C/T snv 1.3E-04 1.0E-04 5
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs770460061 0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14