Disease: Gilbert Disease (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4124874
UGT1A5 ; UGT1A4 ; UGT1A7 ; LOC100286922 ; UGT1A8 ; UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A9
0.851 0.120 2 233757013 intron variant T/A;G snv 8
rs34993780
UGT1A10 ; MROH2A ; UGT1A7 ; UGT1A5 ; UGT1A6 ; UGT1A1 ; UGT1A9 ; UGT1A8 ; UGT1A3 ; UGT1A4
0.827 0.120 2 233772413 missense variant T/A;C;G snv 2.2E-04 7
rs34946978
UGT1A3 ; UGT1A4 ; UGT1A9 ; UGT1A5 ; UGT1A7 ; UGT1A1 ; UGT1A6 ; UGT1A10 ; UGT1A8
0.851 0.120 2 233768226 missense variant C/G;T snv 1.2E-03 6
rs4148326
UGT1A5 ; UGT1A9 ; UGT1A6 ; UGT1A8 ; UGT1A10 ; UGT1A4 ; UGT1A3 ; UGT1A1 ; UGT1A7
0.925 0.080 2 233764816 intron variant T/C snv 0.49 5
rs281865418
UGT1A5 ; UGT1A6 ; UGT1A3 ; UGT1A9 ; UGT1A1 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A4
0.882 0.080 2 233761127 stop gained C/A;G snv 3
rs72551349
UGT1A6 ; UGT1A5 ; UGT1A3 ; UGT1A9 ; UGT1A1 ; UGT1A4 ; UGT1A7 ; UGT1A8 ; UGT1A10
0.925 0.080 2 233767873 stop gained C/G;T snv 4.0E-06; 2.8E-05 2