Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs389883 0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 6
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs437179 0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs659445 0.882 0.160 6 31896527 intron variant G/A;C snv 0.77 0.76 3
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs802791 0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs708035 0.925 0.120 3 10234479 missense variant T/A snv 0.73 0.70 2
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
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82