Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 12
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 11
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs1194338 0.925 0.080 11 65493967 upstream gene variant C/A;T snv 3
rs180040 0.882 0.120 15 97027933 intergenic variant T/C snv 0.85 3
rs7163702 0.925 0.080 15 28460135 upstream gene variant C/A snv 2
rs722025 0.925 0.080 5 8107899 intergenic variant A/G snv 0.27 2
rs823920 0.925 0.080 9 101900303 intergenic variant A/G snv 0.12 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