Disease: Hepatitis B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12304647
MIR196A2 ; HOXC6
0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15
rs3820998
TANK ; LOC105373719
0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs747432300
GPT ; LOC101928953
0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 2
rs2234671
CXCR1
0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54