Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs988344
MROH2A
2 233812088 intron variant A/C;T snv 2
rs9808231
MROH2A
2 233799506 intron variant C/G;T snv 2
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs9287649
MROH2A
2 233781184 intron variant C/G snv 0.15 2
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs879665
MROH2A
2 233831490 missense variant G/A snv 0.15 0.17 2
rs871514
UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A7 ; UGT1A8 ; UGT1A5
2 233719883 intron variant T/C snv 0.54 3
rs869283
UGT1A7 ; UGT1A4 ; UGT1A6 ; UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A8
2 233717641 intron variant G/A snv 0.48 3
rs838736
DGKD
2 233415586 intron variant G/A snv 0.61 2
rs838718
DGKD
2 233388004 intron variant G/A snv 0.50 2
rs838717
DGKD
2 233387798 intron variant G/A snv 0.64 2
rs838716
DGKD
2 233386145 non coding transcript exon variant G/C;T snv 2
rs838709
DGKD
2 233376098 intron variant C/A;T snv 2
rs838708
DGKD
2 233375753 intron variant G/A snv 0.74 2
rs838705
DGKD
2 233364596 intron variant G/A;C snv 2
rs8330
UGT1A4 ; UGT1A7 ; UGT1A6 ; UGT1A9 ; UGT1A10 ; UGT1A5 ; UGT1A3 ; UGT1A1 ; UGT1A8 ; MROH2A
1.000 0.040 2 233772999 3 prime UTR variant G/C snv 0.72 2
rs7969341
SLCO1B1
12 21232670 intron variant A/G snv 0.22 2
rs766420
TKTL1
X 154326058 intron variant C/G snv 0.32 2
rs766419
TKTL1
X 154326315 intron variant A/G snv 0.31 2
rs7608713
UGT1A10 ; UGT1A8
2 233658405 intron variant G/A snv 0.28 2
rs7608175
UGT1A6 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A9
2 233690443 intron variant C/G snv 0.39 3
rs7604115
UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A4
2 233749470 intron variant C/T snv 0.37 3
rs7598771
DGKD
2 233379402 intron variant T/C snv 0.12 2
rs7597496
UGT1A6 ; RPL17P11 ; UGT1A8 ; UGT1A4 ; UGT1A5 ; UGT1A7 ; UGT1A9 ; UGT1A10
2 233721797 non coding transcript exon variant A/C;G snv 3
rs7596785
MROH2A
2 233785531 intron variant T/C;G snv 2