Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs5010528
HLA-B ; HLA-C
0.827 0.240 6 31273255 intron variant A/G snv 0.15 9
rs11568350
SLC40A1
0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs535915558
PMEL
0.827 0.120 12 55958494 missense variant C/T snv 2.0E-05 6
rs56061981
CXCL10 ; ART3
0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 5
rs40837
IL27
0.925 0.120 16 28499524 3 prime UTR variant A/G snv 0.43 5
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs12662869
SLC17A1
0.925 0.120 6 25784253 intron variant C/A snv 0.34 4
rs4148324
UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A4 ; UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A5 ; UGT1A1
2 233764076 intron variant T/A;G snv 0.36 4
rs6714634
UGT1A3 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A7 ; LOC100286922 ; UGT1A5 ; UGT1A9 ; UGT1A4
2 233756119 non coding transcript exon variant T/C snv 0.30 4
rs10179091
UGT1A4 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9
2 233749337 intron variant T/C snv 0.49 4
rs10178992
UGT1A5 ; UGT1A3 ; UGT1A10 ; UGT1A8 ; UGT1A4 ; UGT1A9 ; UGT1A7 ; UGT1A6
2 233749231 intron variant T/A snv 0.37 4
rs17862875
UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A9 ; UGT1A4 ; UGT1A7
2 233740656 intron variant G/A snv 0.30 4
rs10929301
UGT1A6 ; UGT1A7 ; UGT1A5 ; UGT1A10 ; LOC100286922 ; UGT1A4 ; UGT1A9 ; UGT1A8 ; UGT1A3
2 233755003 splice region variant C/G;T snv 0.48 4
rs10929302
UGT1A7 ; UGT1A9 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; LOC100286922 ; UGT1A4
2 233757136 intron variant G/A snv 0.30 4
rs11673726
UGT1A8 ; LOC100286922 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A9 ; UGT1A4
2 233755414 non coding transcript exon variant G/A;T snv 4
rs11888459
UGT1A8 ; UGT1A5 ; UGT1A2P ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A9
2 233747994 non coding transcript exon variant T/C snv 0.37 4
rs7604115
UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A4
2 233749470 intron variant C/T snv 0.37 4
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs2255301
CD4
0.925 0.160 12 6800276 intron variant T/C snv 0.59 0.61 3
rs11695484
DNAJB3 ; UGT1A3 ; UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A5
2 233745803 intron variant A/G snv 0.30 3