Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35982104
UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9
2 233698914 intron variant -/T ins 2
rs2602362 2 233607902 downstream gene variant A/C snv 0.22 3
rs4663967
UGT1A9 ; UGT1A5 ; UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; DNAJB3 ; UGT1A4 ; UGT1A6
2 233744538 intron variant A/C snv 0.55 3
rs6753320
UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
2 233686969 intron variant A/C snv 0.39 3
rs6753569
UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A10
2 233687171 intron variant A/C snv 0.39 3
rs10841645 12 20795800 intergenic variant A/C snv 0.59 2
rs11045611
SLCO1B3-SLCO1B7
12 20946338 intron variant A/C snv 0.14 2
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 2
rs12988520
UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
1.000 0.040 2 233698748 intron variant A/C snv 0.51 2
rs17862836 2 233606117 downstream gene variant A/C snv 0.20 2
rs2602372
UGT1A8 ; UGT1A10
2 233644668 intron variant A/C snv 2.0E-02 2
rs4663754 2 233605074 downstream gene variant A/C snv 0.21 2
rs6728792 2 233600046 upstream gene variant A/C snv 0.22 2
rs6754100
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A8
2 233687568 intron variant A/C snv 0.68 2
rs6761246
UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A10
2 233694793 intron variant A/C snv 0.65 2
rs17864683
UGT1A10 ; UGT1A8 ; UGT1A9
2 233670563 intron variant A/C;G snv 3
rs7597496
UGT1A6 ; RPL17P11 ; UGT1A8 ; UGT1A4 ; UGT1A5 ; UGT1A7 ; UGT1A9 ; UGT1A10
2 233721797 non coding transcript exon variant A/C;G snv 3
rs17868378 2 233899733 intergenic variant A/C;G snv 2
rs1901815
UGT1A10 ; UGT1A8
2 233663168 intron variant A/C;G snv 0.97 2
rs28898605
UGT1A4 ; UGT1A5 ; UGT1A7 ; UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A8
2 233716848 intron variant A/C;G snv 2
rs6722763
DGKD
2 233373564 intron variant A/C;G snv 2
rs3755319
UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6
0.925 0.120 2 233758936 intron variant A/C;G;T snv 3
rs6760588
UGT1A10 ; UGT1A8
2 233664137 intron variant A/C;G;T snv 2
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 3
rs988344
MROH2A
2 233812088 intron variant A/C;T snv 2