Disease: Leukopenia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs1448674651
TYMS ; ENOSF1
0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs4149117
SLCO1B3-SLCO1B7 ; SLCO1B3
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs67376798
DPYD
0.851 0.120 1 97082391 missense variant T/A snv 2.8E-03 3.3E-03 9
rs4124874
UGT1A5 ; UGT1A4 ; UGT1A7 ; LOC100286922 ; UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A9
0.851 0.120 2 233757013 intron variant T/A;G snv 8
rs7311358
SLCO1B3-SLCO1B7 ; SLCO1B3
0.827 0.160 12 20862826 missense variant G/A snv 0.81 0.72 6
rs2032592
DDX3Y
0.851 0.160 Y 12919473 3 prime UTR variant A/G snv 1.6E-04 5
rs1801019
UMPS
0.882 0.080 3 124737895 missense variant G/A;C snv 4.0E-06; 0.19 4
rs2244613
CES1
0.882 0.120 16 55810697 intron variant G/A;T snv 8.0E-06; 0.73 4
rs1050274678
SLC19A1
0.925 0.040 21 45530803 missense variant C/T snv 1.1E-05 7.0E-06 3
rs17376848
DPYD
0.925 0.040 1 97450068 synonymous variant A/G snv 5.1E-02 4.3E-02 3
rs3758581
CYP2C19
0.925 0.040 10 94842866 missense variant A/G snv 0.95 3
rs72552763
SLC22A1
0.925 0.040 6 160139849 inframe deletion GAT/- delins 0.15 3