Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs931127 0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs4461062 1.000 0.080 16 56830706 intron variant C/T snv 0.48 0.48 2
rs1347591 1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47 2
rs4442975 0.827 0.120 2 217056046 intergenic variant G/T snv 0.47 7
rs1040411 1.000 0.120 6 106150148 intron variant G/A snv 0.47 3
rs992157 0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 2
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs653765 0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs9879947 3 108046545 3 prime UTR variant G/A snv 0.45 1
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 15
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs946486 9 130770618 intron variant C/T snv 0.44 1
rs8103851 0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 15
rs5780218 0.882 0.080 1 204196482 5 prime UTR variant A/- delins 0.44 4
rs6024836 0.851 0.160 20 56369012 downstream gene variant G/A snv 0.42 6
rs6464926 0.882 0.120 7 148821919 intron variant C/T snv 0.41 4
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1478604 0.807 0.240 15 39581120 5 prime UTR variant T/C snv 0.40 8
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55