Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1128249 1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs459193 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs863750 12 124020897 intron variant C/T snv 0.53 7
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs1358980 6 43796814 intergenic variant C/T snv 0.40 6
rs1045241 1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs9991328 4 88791970 intron variant C/T snv 0.53 5