Disease: Hepatitis B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7755596 0.882 0.280 6 32738701 upstream gene variant C/T snv 0.80 3
rs7756516
HLA-DQB2
0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 4
rs7773694 0.882 0.280 6 32738557 upstream gene variant A/G snv 0.80 3
rs8179673
STAT4
0.882 0.240 2 191104615 intron variant C/G;T snv 3
rs9268615 0.882 0.280 6 32435112 upstream gene variant G/A snv 0.38 3
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs9276162 0.882 0.280 6 32730680 downstream gene variant G/A snv 0.74 3
rs9276370
HLA-DQA2
0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 3
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14