Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs11563251
UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A5 ; UGT1A1 ; UGT1A4 ; UGT1A10 ; UGT1A8
2 233770738 3 prime UTR variant C/T snv 0.19 5
rs11891311
UGT1A8 ; UGT1A3 ; UGT1A5 ; UGT1A9 ; UGT1A10 ; UGT1A4 ; UGT1A6 ; UGT1A7
2 233730664 intron variant G/A snv 0.42 4
rs1550532
DGKD
2 233356202 intron variant C/G snv 0.75 4
rs10167119
UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
2 233680666 intron variant T/C snv 0.34 3
rs10168155
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10
2 233688190 intron variant C/T snv 0.39 3
rs10168333
UGT1A10 ; UGT1A9 ; UGT1A8 ; UGT1A7
2 233688342 intron variant C/T snv 0.39 3
rs10171367
UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A10
2 233689021 intron variant C/A;G snv 3
rs10175809
UGT1A10 ; UGT1A7 ; UGT1A8 ; UGT1A9
2 233688219 intron variant T/A snv 0.39 3
rs10178992
UGT1A5 ; UGT1A3 ; UGT1A10 ; UGT1A8 ; UGT1A4 ; UGT1A9 ; UGT1A7 ; UGT1A6
2 233749231 intron variant T/A snv 0.37 3
rs10179091
UGT1A4 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9
2 233749337 intron variant T/C snv 0.49 3
rs10179094
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
2 233689179 intron variant T/A snv 0.34 3
rs10197460
UGT1A10 ; UGT1A9 ; UGT1A8 ; UGT1A7
2 233680544 intron variant G/T snv 0.34 3
rs10445704
UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A8
2 233691628 5 prime UTR variant G/A snv 0.39 3
rs10929301
UGT1A6 ; UGT1A7 ; UGT1A5 ; UGT1A10 ; LOC100286922 ; UGT1A4 ; UGT1A9 ; UGT1A8 ; UGT1A3
2 233755003 splice region variant C/G;T snv 0.48 3
rs10929302
UGT1A7 ; UGT1A9 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; LOC100286922 ; UGT1A4
2 233757136 intron variant G/A snv 0.30 3
rs11673726
UGT1A8 ; LOC100286922 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A9 ; UGT1A4
2 233755414 non coding transcript exon variant G/A;T snv 3
rs11680450
UGT1A8 ; UGT1A9 ; UGT1A10 ; UGT1A7
2 233688837 intron variant T/A;C snv 3
rs11694406
DGKD
2 233423164 intron variant G/A snv 0.12 3
rs11888459
UGT1A8 ; UGT1A5 ; UGT1A2P ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A9
2 233747994 non coding transcript exon variant T/C snv 0.37 3
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 3
rs11902131
UGT1A8 ; UGT1A7 ; UGT1A10 ; UGT1A9
2 233685623 intron variant C/T snv 0.39 3
rs12623271
UGT1A6 ; UGT1A8 ; UGT1A10 ; UGT1A9 ; UGT1A7
2 233691295 3 prime UTR variant C/G snv 0.39 3
rs13002774
UGT1A10 ; UGT1A9 ; UGT1A8 ; UGT1A7
2 233685060 intron variant G/A;T snv 3