Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs4841132 8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs10127775 1 230160042 intron variant A/G;T snv 4
rs2657880 12 56469986 3 prime UTR variant G/C snv 0.15 4