Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6577555 1.000 0.080 1 9152228 intron variant A/C snv 0.74 1
rs1537378 0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs776746 0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs705381 1.000 0.080 7 95324637 upstream gene variant T/C snv 0.72 2
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs17669 0.851 0.160 18 58451261 non coding transcript exon variant C/A;T snv 0.72 5
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2020918 0.925 0.080 8 42214920 intergenic variant A/G snv 0.71 2
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6843082 0.925 0.120 4 110796911 non coding transcript exon variant G/A snv 0.71 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs9860747 0.925 0.080 3 186869628 regulatory region variant T/C snv 0.70 2
rs1330344 0.925 0.120 9 122369409 upstream gene variant C/T snv 0.69 2
rs1764390 0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs4846048 0.752 0.280 1 11786195 3 prime UTR variant G/A snv 0.67 10
rs7136446 0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs288980 1.000 0.080 18 21029619 intron variant T/C snv 0.66 1
rs1256065 0.925 0.120 14 64232214 3 prime UTR variant G/T snv 0.66 3
rs2634074 1.000 0.080 4 110755885 intergenic variant T/A snv 0.66 1
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs3826392 0.827 0.200 17 12019587 intron variant G/T snv 0.65 5
rs982873 0.925 0.160 13 90145678 intergenic variant T/C snv 0.65 2
rs751357 1.000 0.080 3 138359313 intron variant T/C snv 0.65 1
rs35196866 1.000 0.080 9 134379472 5 prime UTR variant C/A snv 0.74 0.65 1