Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs2243191
LOC105372878 ; IL19
1.000 0.040 1 206842612 missense variant T/C;G snv 0.71; 5.5E-06 2
rs396716
FCGR3A
1 161544806 missense variant A/G snv 7.2E-05 6.3E-05 1
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs11568350
SLC40A1
0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
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
rs201565523
SLC11A1
0.925 0.240 2 218390027 missense variant C/T snv 2.9E-04 7.7E-05 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