Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 5
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 3
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
rs1574560 1.000 0.120 3 166329716 intergenic variant T/C snv 0.42 1
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs8044477 1.000 0.120 16 58942687 intron variant A/G snv 0.53 1
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs533117495
ABCB1
0.827 0.200 7 87595783 missense variant C/T snv 8.0E-06 5
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11 2
rs927062
AKAP6
0.925 0.120 14 32625843 intron variant A/G snv 0.22 2
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2
rs2256787
ARHGEF10L
0.925 0.120 1 17566321 intron variant A/C snv 0.93 2
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs370681
AXIN1
0.807 0.200 16 342461 intron variant C/T snv 0.48 6