Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs8175347
UGT1A9 ; UGT1A1 ; UGT1A6 ; UGT1A10 ; UGT1A8 ; UGT1A3 ; UGT1A5 ; UGT1A7 ; UGT1A4
0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs4124874
UGT1A5 ; UGT1A4 ; UGT1A7 ; LOC100286922 ; UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A9
0.851 0.120 2 233757013 intron variant T/A;G snv 8
rs4533622
CTNNB1
0.807 0.240 3 41200847 intron variant C/A;T snv 6
rs149104283
SLCO1B3-SLCO1B7
0.882 0.040 12 20930928 intron variant C/G;T snv 4
rs2244613
CES1
0.882 0.120 16 55810697 intron variant G/A;T snv 8.0E-06; 0.73 4
rs2305482
PSMD3
0.851 0.200 17 39984674 intron variant A/C snv 0.57 4
rs2916733
MCPH1
0.851 0.120 8 6465757 intron variant G/A snv 0.28 4
rs4240803
SLC7A5 ; LOC107987237
0.851 0.240 16 87855597 intron variant G/A;C;T snv 4
rs9561778
ABCC4
0.851 0.120 13 95061461 intron variant G/A;T snv 4
rs11141915
DAPK1
0.882 0.160 9 87620879 intron variant A/C snv 0.25 3
rs11706052
IMPDH2
0.882 0.080 3 49026677 intron variant A/G snv 8.3E-02 7.6E-02 3
rs2074087
ABCC1
0.882 0.080 16 16090375 intron variant C/G snv 0.81 0.83 3
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02 2
rs17501331
ABCC1
0.925 0.040 16 15995584 intron variant A/G snv 7.7E-02 2
rs2074549
VCP
0.925 0.040 9 35061506 intron variant T/A;C snv 2
rs3136228
MSH6
0.925 0.040 2 47782677 intron variant T/G snv 0.30 2
rs3825876
SLC28A1
0.925 0.040 15 84892637 intron variant G/A snv 0.34 2
rs4148396
ABCC2
0.925 0.040 10 99832187 intron variant T/C snv 0.65 2
rs4987219
SLC23A2
0.925 0.080 20 4884300 intron variant C/G;T snv 2
rs693955
SLC29A1
0.925 0.040 6 44224183 intron variant A/C snv 0.85 2
rs7091672 0.925 0.040 10 118836909 intron variant T/A;C;G snv 2
rs747199
SLC29A1
0.925 0.040 6 44226608 intron variant G/C snv 0.15 2