Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3758581
CYP2C19
0.925 0.040 10 94842866 missense variant A/G snv 0.95 3
rs654448
RAD18
1.000 0.040 3 8893530 intron variant C/T snv 0.85 1
rs693955
SLC29A1
0.925 0.040 6 44224183 intron variant A/C snv 0.85 2
rs2074087
ABCC1
0.882 0.080 16 16090375 intron variant C/G snv 0.81 0.83 3
rs586014
RAD18
1.000 0.040 3 8965408 upstream gene variant A/G snv 0.82 1
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs7311358
SLCO1B3-SLCO1B7 ; SLCO1B3
0.827 0.160 12 20862826 missense variant G/A snv 0.81 0.72 6
rs4148396
ABCC2
0.925 0.040 10 99832187 intron variant T/C snv 0.65 2
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs6498588
LOC107984869
0.925 0.040 16 15938949 intergenic variant A/T snv 0.65 2
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1901440 0.925 0.040 2 133680388 intergenic variant C/A snv 0.58 2
rs1885301
ABCC2
0.925 0.040 10 99781296 upstream gene variant A/G snv 0.58 2
rs7438135
UGT2B7
1.000 0.040 4 69095621 intron variant G/A snv 0.58 1
rs1135840
NDUFA6-DT ; CYP2D6
0.807 0.200 22 42126611 missense variant C/G snv 0.58 8
rs2305482
PSMD3
0.851 0.200 17 39984674 intron variant A/C snv 0.57 4
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs11719165 0.925 0.040 3 194865359 intergenic variant T/C snv 0.53 2
rs1110277
SLC23A2
0.925 0.080 20 4874036 synonymous variant A/G snv 0.34 0.43 2
rs2273626
HAUS4 ; MIR4707
0.925 0.120 14 22956973 mature miRNA variant C/A snv 0.58 0.41 2
rs4737420
LYN
0.925 0.080 8 55895622 non coding transcript exon variant T/C snv 0.38 3
rs2278294
IMPDH1
0.882 0.080 7 128400645 non coding transcript exon variant C/T snv 0.38 3
rs9990999
DCTD
0.925 0.040 4 182902820 intron variant G/A snv 0.37 2