Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79002828 0.925 0.040 5 44318015 intron variant A/G snv 9.6E-03 2
rs8027411 0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs9318086 0.882 0.040 13 23858328 intron variant A/G snv 0.55 3
rs5742632 0.851 0.120 12 102462696 intron variant A/G snv 0.26 4
rs2946834 0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26