Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10178992
UGT1A5 ; UGT1A3 ; UGT1A10 ; UGT1A8 ; UGT1A4 ; UGT1A9 ; UGT1A7 ; UGT1A6
2 233749231 intron variant T/A snv 0.37 4
rs10179091
UGT1A4 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9
2 233749337 intron variant T/C snv 0.49 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
rs17862875
UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A9 ; UGT1A4 ; UGT1A7
2 233740656 intron variant G/A snv 0.30 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
rs7604115
UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A4
2 233749470 intron variant C/T snv 0.37 4
rs11695484
DNAJB3 ; UGT1A3 ; UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A5
2 233745803 intron variant A/G snv 0.30 3
rs17864701
UGT1A4 ; UGT1A3 ; UGT1A6 ; UGT1A8 ; UGT1A7 ; UGT1A5 ; DNAJB3 ; UGT1A9 ; UGT1A10
2 233744071 intron variant C/T snv 0.30 3
rs3771341
UGT1A4 ; UGT1A10 ; UGT1A6 ; UGT1A3 ; UGT1A5 ; UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A1
2 233764593 intron variant G/A;T snv 0.33 3
rs6747843
UGT1A10 ; UGT1A8 ; UGT1A6 ; UGT1A5 ; UGT1A4 ; LOC100286922 ; UGT1A9 ; UGT1A7 ; UGT1A3
2 233755708 non coding transcript exon variant G/A snv 0.30 3
rs10041590
C5orf17
5 24064827 intron variant T/C;G snv 2
rs10054178
C5orf17
5 24059742 intron variant A/G snv 7.5E-02 2
rs10056373
C5orf17
5 24069684 intron variant C/T snv 7.4E-02 2
rs10119043 9 135122706 downstream gene variant C/T snv 0.11 2
rs10827209
NRP1
10 33198261 intron variant A/C snv 0.23 2
rs10892961
CLMP
11 123093392 intron variant A/C;G;T snv 2
rs11011237
TACC1P1
10 37531016 intron variant G/A snv 9.2E-02 2
rs11218976
CLMP
11 123090950 intron variant A/G snv 0.41 2
rs11228672
OR5M13P
11 56597931 non coding transcript exon variant G/A;C snv 2
rs113051092
C5orf17
5 24060490 intron variant A/T snv 7.4E-02 2
rs116965780 18 43300829 intergenic variant C/T snv 7.0E-02 2