Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2289263 0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs6494629 0.925 0.120 15 67081773 intron variant C/T snv 0.52 2
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140