Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1127313 1.000 0.120 1 154583949 3 prime UTR variant G/A snv 0.41 1
rs1017134 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 2
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs142091544 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 2
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 2
rs7501462 0.925 0.120 17 16974091 upstream gene variant A/G snv 0.31 2
rs1955513 0.925 0.120 14 32706736 intron variant T/G snv 0.11 2
rs927062 0.925 0.120 14 32625843 intron variant A/G snv 0.22 2
rs10788679 0.925 0.120 1 17590467 intron variant A/G snv 0.59 2
rs2256787 0.925 0.120 1 17566321 intron variant A/C snv 0.93 2
rs7572644 0.925 0.120 2 28097166 intron variant T/C snv 0.21 2
rs9609538 0.925 0.120 22 32413845 upstream gene variant T/C snv 0.34 2
rs1983383 0.925 0.120 2 30754766 intron variant C/A snv 0.39 2
rs41324349 0.925 0.120 7 2907529 intron variant G/A;C;T snv 2
rs3769827 0.925 0.120 2 201237962 intron variant A/G snv 0.42 2
rs17507066 0.925 0.120 22 28696732 intron variant C/T snv 7.0E-02 2
rs1413299 0.925 0.120 9 98998959 intron variant G/A;T snv 2
rs561841834 0.925 0.120 21 45468531 synonymous variant C/T snv 8.0E-06 2
rs114972508 0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 2
rs7053448
F8
0.925 0.120 X 154964936 intron variant T/C snv 0.15 2
rs7058826
F8
0.925 0.120 X 154966714 intron variant C/T snv 0.12 0.14 2
rs17702471 0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16 2
rs2190503 0.925 0.120 7 50674920 intron variant A/G;T snv 2
rs17427875 0.925 0.120 7 27185939 non coding transcript exon variant A/T snv 0.15 2
rs3745546 0.925 0.120 19 7211805 intron variant G/A;C snv 2