Disease: Hepatitis B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs1054690270
LOC101928953 ; GPT
0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs1419881
TCF19
0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 4
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs3759333
LTBR
0.882 0.120 12 6382781 intron variant C/G;T snv 3
rs3806798
IL15
0.925 0.080 4 141636126 upstream gene variant T/A snv 8.7E-02 2
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs7095891
MBL2
0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 3
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7756516
HLA-DQB2
0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 4
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60