Disease: Hepatitis B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs10918706
CD247
0.925 0.200 1 167496884 intron variant C/T snv 0.24 2
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs13199787 0.925 0.200 6 32737499 upstream gene variant C/T snv 0.38 2
rs1383265 0.925 0.200 6 32772111 intergenic variant T/A;C snv 2
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2051549
HLA-DQB2
0.851 0.280 6 32762309 intron variant G/A snv 0.64 4
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2301271
HLA-DQB2
0.882 0.240 6 32757416 intron variant A/G snv 0.60 3
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2523454
MICA-AS1 ; MICA
0.882 0.240 6 31400088 5 prime UTR variant G/A snv 0.22 3
rs2647050 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 4
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193