Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
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
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 5
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs7313833 0.851 0.120 12 27930263 intergenic variant G/A snv 0.37 4
rs4954956 0.882 0.120 2 138787007 regulatory region variant C/T snv 0.25 3
rs7365052 0.882 0.120 1 236786561 intergenic variant T/C snv 3
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
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
rs2229109
ABCB1
0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02 8
rs533117495
ABCB1
0.827 0.200 7 87595783 missense variant C/T snv 8.0E-06 5
rs35068177
ABCB1
0.882 0.120 7 87550213 synonymous variant T/C snv 2.2E-04 3.1E-04 3
rs1127313
ADAR ; CHRNB2
1.000 0.120 1 154583949 3 prime UTR variant G/A snv 0.41 1
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs1955513
AKAP6
0.925 0.120 14 32706736 intron variant T/G snv 0.11 2