Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs5888 0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11