Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4795519 1.000 0.080 17 27214252 intergenic variant A/C snv 0.43 1
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
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
rs4148356
ABCC1
0.851 0.120 16 16083418 missense variant G/A snv 2.3E-02 1.3E-02 4
rs45511401
ABCC1
0.851 0.120 16 16079375 missense variant G/T snv 3.8E-02 3.6E-02 4
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs2273697
ABCC2
0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 11
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs1057519771
ABL1
1.000 0.080 9 130872201 missense variant G/C snv 2
rs121913454
ABL1
0.925 0.080 9 130874969 missense variant A/G snv 2
rs121913460
ABL1
0.925 0.080 9 130862971 missense variant A/T snv 2
rs1314838108
ABL1
0.925 0.160 9 130854977 missense variant G/A snv 7.0E-06 2
rs1057519758
ABL1
1.000 0.080 9 130872153 missense variant T/G snv 1
rs1057519772
ABL1
1.000 0.080 9 130872895 missense variant A/G snv 1
rs1057519774
ABL1
1.000 0.080 9 130872902 missense variant T/G snv 1