Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs2188962 0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs1847472 0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 3