Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10272724 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 4
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs7789635 0.882 0.120 7 50405912 downstream gene variant T/C snv 0.40 4
rs6944602 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 2
rs17015014 1.000 0.120 4 141807619 regulatory region variant G/C snv 0.16 1
rs35964658 1.000 0.120 4 141758435 intergenic variant A/G snv 8.6E-02 1
rs6140264 1.000 0.120 20 7395707 intergenic variant G/A snv 0.15 1
rs9901160 1.000 0.120 17 18371829 TF binding site variant G/A snv 0.19 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
rs2229109
ABCB1
0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02 8
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs979090956
ABCB1
0.827 0.200 7 87553822 missense variant G/C snv 5
rs200378616
ABCB1
0.882 0.120 7 87544938 missense variant G/C;T snv 4.0E-05; 8.0E-06 3
rs3213619
ABCB1
1.000 0.120 7 87600877 5 prime UTR variant A/G snv 5.2E-02 1
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
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
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7