Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1461494 11 123055777 downstream gene variant T/A;C snv 2
rs7154653
RIN3
14 92577033 intron variant T/A;C snv 1
rs10178992
UGT1A5 ; UGT1A3 ; UGT1A10 ; UGT1A8 ; UGT1A4 ; UGT1A9 ; UGT1A7 ; UGT1A6
2 233749231 intron variant T/A snv 0.37 4
rs113162402
SEPTIN4-AS1 ; SEPTIN4
17 58522103 splice acceptor variant T/A snv 1
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs3091250
CCR3
1.000 0.040 3 46264639 non coding transcript exon variant G/T snv 0.26 2
rs765009973
CCR5AS ; CCR5
3 46373909 missense variant G/T snv 7.4E-05 2.1E-05 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2866233
EMCN
4 100649444 intron variant G/C;T snv 1
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs7047901
OLFM1
9 135121569 downstream gene variant G/C snv 0.11 2
rs11673726
UGT1A8 ; LOC100286922 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A9 ; UGT1A4
2 233755414 non coding transcript exon variant G/A;T snv 4
rs3771341
UGT1A4 ; UGT1A10 ; UGT1A6 ; UGT1A3 ; UGT1A5 ; UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A1
2 233764593 intron variant G/A;T snv 0.33 3
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs34003842
DLGAP2
8 1206131 intron variant G/A;C;T snv 2
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs11228672
OR5M13P
11 56597931 non coding transcript exon variant G/A;C snv 2
rs17062789
DLGAP2
8 1203198 intron variant G/A;C snv 2
rs11087114
MACROD2-AS1 ; MACROD2
20 14931037 intron variant G/A;C snv 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs10929302
UGT1A7 ; UGT1A9 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; LOC100286922 ; UGT1A4
2 233757136 intron variant G/A snv 0.30 4
rs17862875
UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A9 ; UGT1A4 ; UGT1A7
2 233740656 intron variant G/A snv 0.30 4
rs6747843
UGT1A10 ; UGT1A8 ; UGT1A6 ; UGT1A5 ; UGT1A4 ; LOC100286922 ; UGT1A9 ; UGT1A7 ; UGT1A3
2 233755708 non coding transcript exon variant G/A snv 0.30 3