Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13162612 0.882 0.080 5 8042908 intergenic variant A/G snv 5.1E-02 3
rs1560642 0.882 0.080 5 148888172 intergenic variant T/C;G snv 3
rs1663689 0.882 0.080 10 8983232 intergenic variant T/C snv 0.25 3
rs1814343 0.882 0.080 11 129695357 regulatory region variant C/T snv 0.22 3
rs2736107 0.882 0.080 5 1297739 upstream gene variant C/T snv 0.23 3
rs2924471 0.882 0.080 5 8055148 intergenic variant T/C snv 0.15 3
rs3742038 0.882 0.080 12 120371388 non coding transcript exon variant A/G snv 0.16 3
rs3856776 0.882 0.080 3 189580619 intergenic variant C/A;G;T snv 3
rs4665162 0.882 0.080 2 160203673 intron variant A/G snv 0.30 3
rs4785367 0.882 0.080 16 49922283 non coding transcript exon variant T/C snv 0.53 3
rs5756523 0.882 0.080 22 37117508 intergenic variant T/A;C snv 3
rs7248167 0.882 0.080 19 43455962 downstream gene variant A/C snv 0.22 3
rs7452888 0.882 0.080 6 169296169 downstream gene variant A/G snv 0.57 3
rs793544 0.882 0.080 3 107368152 intron variant T/C snv 0.35 3
rs7959801 0.882 0.080 12 120371787 upstream gene variant T/C snv 0.37 3
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
rs3842
ABCB1
0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16 5
rs149518139
ABCB1
0.882 0.080 7 87566852 missense variant T/C snv 4.0E-06 3
rs2188524
ABCB1
0.882 0.080 7 87601119 intron variant T/C snv 3.2E-03 3
rs2235013
ABCB1
0.882 0.080 7 87549310 intron variant C/T snv 0.46 0.48 3
rs212091
ABCC1
0.827 0.120 16 16142793 3 prime UTR variant T/A;C snv 5
rs4148356
ABCC1
0.851 0.120 16 16083418 missense variant G/A snv 2.3E-02 1.3E-02 4
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56