Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3749147 0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs4665963 0.925 0.120 2 27305824 splice region variant T/C snv 0.35 0.43 3
rs714052 0.925 0.120 7 73450539 intron variant A/G snv 9.2E-02 4
rs7586601 0.925 0.120 2 27361799 intron variant A/G snv 0.54 3
rs780090 0.925 0.120 2 27495607 upstream gene variant T/C;G snv 4
rs780092 0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs7800944 0.882 0.160 7 73621527 intron variant T/C snv 0.28 4
rs799166 0.925 0.120 7 73637602 intergenic variant C/G snv 0.16 4
rs813592 0.925 0.120 2 27499104 intron variant T/C snv 0.42 0.47 3
rs814295 0.925 0.120 2 27520348 intron variant A/G snv 0.18 5