Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 22
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 9
rs4124874
UGT1A5 ; UGT1A4 ; UGT1A7 ; LOC100286922 ; UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A9
0.851 0.120 2 233757013 intron variant T/A;G snv 8
rs3755319
UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6
0.925 0.120 2 233758936 intron variant A/C;G;T snv 8
rs6759892
UGT1A6 ; UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
0.851 0.160 2 233693023 missense variant T/G snv 0.39 0.39 7
rs1875263
UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A8 ; UGT1A4
1.000 2 233716976 intron variant C/G;T snv 7
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs4663969
UGT1A6 ; UGT1A9 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A4 ; UGT1A8 ; UGT1A7
1.000 2 233746667 intron variant C/A;T snv 6
rs10203853
MROH2A
1.000 0.080 2 233778772 intron variant A/G;T snv 5
rs6728940
MROH2A
1.000 0.080 2 233780518 intron variant G/A snv 0.26 5
rs4149000
SLCO1A2
0.882 0.080 12 21295063 non coding transcript exon variant C/T snv 0.11 5
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 5
rs4363657
SLCO1B1
12 21215788 intron variant T/C snv 0.18 5
rs10929251
UGT1A10 ; UGT1A8
1.000 0.080 2 233637583 intron variant A/G snv 0.13 5
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 5
rs17864678
UGT1A10 ; UGT1A8
1.000 0.080 2 233635964 intron variant T/A snv 5.6E-03 5
rs4148326
UGT1A5 ; UGT1A9 ; UGT1A6 ; UGT1A8 ; UGT1A10 ; UGT1A4 ; UGT1A3 ; UGT1A1 ; UGT1A7
0.925 0.080 2 233764816 intron variant T/C snv 0.49 5
rs11563251
UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A5 ; UGT1A1 ; UGT1A4 ; UGT1A10 ; UGT1A8
2 233770738 3 prime UTR variant C/T snv 0.19 5