Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368234815
IFNL4
0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs1966678 4 29322410 intergenic variant T/G snv 0.60 2
rs4761669 12 94793846 intergenic variant T/G snv 0.27 1
rs10041590
C5orf17
5 24064827 intron variant T/C;G snv 2
rs2243191
LOC105372878 ; IL19
1.000 0.040 1 206842612 missense variant T/C;G snv 0.71; 5.5E-06 2
rs73670671
DLGAP2
8 1203645 intron variant T/C;G snv 2
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 15
rs10179091
UGT1A4 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9
2 233749337 intron variant T/C snv 0.49 4
rs11888459
UGT1A8 ; UGT1A5 ; UGT1A2P ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A9
2 233747994 non coding transcript exon variant T/C snv 0.37 4
rs6714634
UGT1A3 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A7 ; LOC100286922 ; UGT1A5 ; UGT1A9 ; UGT1A4
2 233756119 non coding transcript exon variant T/C snv 0.30 4
rs2227513
LOC105369818 ; IL22
1.000 0.080 12 68253559 intron variant T/C snv 0.15 3
rs2255301
CD4
0.925 0.160 12 6800276 intron variant T/C snv 0.59 0.61 3
rs1836778 4 29332870 intergenic variant T/C snv 0.56 2
rs34352510
UGT1A9 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A5 ; UGT1A8 ; UGT1A4
2 233741916 non coding transcript exon variant T/C snv 0.33 2
rs6139258
RNF24
1.000 0.080 20 3977969 intron variant T/C snv 3.2E-02 2
rs6448638 4 29333941 intergenic variant T/C snv 0.56 2
rs7039098
OLFM1
9 135121473 downstream gene variant T/C snv 0.11 2
rs72749479 9 80667356 intergenic variant T/C snv 8.5E-02 2
rs72749483 9 80670259 intergenic variant T/C snv 8.5E-02 2
rs2280828 8 117750197 intergenic variant T/C snv 4.2E-02 1
rs75158213 3 48345739 intergenic variant T/C snv 1.2E-02 1
rs4148324
UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A4 ; UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A5 ; UGT1A1
2 233764076 intron variant T/A;G snv 0.36 4
rs2907092
CTNND2
5 11047569 intron variant T/A;G snv 1