Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4288398 1.000 0.120 8 7024116 downstream gene variant A/G snv 0.70 1
rs4646 0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs7763262 1.000 0.120 6 32457105 downstream gene variant T/C snv 0.70 1
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs4227 1.000 0.120 17 7587859 3 prime UTR variant G/T snv 0.71 0.67 2
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs12022418 1.000 0.120 1 192565977 intron variant C/A snv 0.64 1
rs3803800 0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs11264794 1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 2
rs9314614 1.000 0.120 8 6840209 intron variant C/G snv 0.61 2
rs1055901 1.000 0.120 18 63805221 3 prime UTR variant T/C snv 0.61 1
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1055902 1.000 0.120 18 63805309 3 prime UTR variant C/T snv 0.59 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2738058 0.925 0.160 8 6964095 upstream gene variant T/C snv 0.57 2
rs2412971 0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs11102930 0.925 0.160 1 115338434 intron variant G/A snv 0.54 2