Disease: Hepatitis B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4656942
CD244
0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618
CD244
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs7536540
MIR101-1 ; MIR3671 ; JAK1
0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs2234671
CXCR1
0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3820998
TANK ; LOC105373719
0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1358379
LINC00472 ; MIR30A
0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11