Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs908832 0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs12493885 1.000 0.040 3 154122077 missense variant G/C snv 0.91 0.91 1
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs352493 0.882 0.040 19 4180839 missense variant C/G;T snv 0.88 3
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs891512 0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs753482 0.925 0.040 7 151009295 intron variant C/A;G;T snv 0.83; 4.0E-05; 3.1E-05; 4.4E-06 3
rs767870 0.882 0.120 12 1780657 intron variant G/A;C snv 0.82 4
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs2298566 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs1250259 1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs35489971 1.000 0.040 17 74704804 missense variant A/G;T snv 0.73 2
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs2168518 0.851 0.160 15 74788737 mature miRNA variant G/A snv 0.71 0.44 4
rs3890011 0.925 0.040 1 46933071 intron variant G/C snv 0.71 0.65 3