Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
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
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs17032980 1.000 0.120 2 67075611 intergenic variant A/G snv 0.25 3
rs4463516 1.000 0.120 9 32867483 intron variant G/C;T snv 3
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs920590 1.000 0.120 8 19793650 regulatory region variant T/C snv 0.39 3
rs11770117 1.000 0.120 7 50406065 downstream gene variant A/T snv 0.41 2
rs12719019 1.000 0.120 7 50408441 downstream gene variant C/T snv 0.40 2
rs6944602 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 2
rs10261922 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 1
rs1110701 1.000 0.120 7 50410929 intergenic variant A/G;T snv 1
rs12887958 1.000 0.120 14 23113360 downstream gene variant C/T snv 0.37 1
rs1569175 1.000 0.120 2 200157231 intergenic variant T/C snv 0.88 1
rs17079534 1.000 0.120 3 39805581 upstream gene variant G/A;C snv 1
rs1945213 1.000 0.120 11 56408195 upstream gene variant C/G;T snv 1
rs4266962 1.000 0.120 10 22052645 intergenic variant C/G;T snv 1
rs4982729 1.000 0.120 14 23107402 upstream gene variant T/C snv 0.66 1
rs4982731 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 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
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
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