Disease: Hepatitis B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
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
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2051549
HLA-DQB2
0.851 0.280 6 32762309 intron variant G/A snv 0.64 4
rs2523454
MICA-AS1 ; MICA
0.882 0.240 6 31400088 5 prime UTR variant G/A snv 0.22 3
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs9268615 0.882 0.280 6 32435112 upstream gene variant G/A snv 0.38 3
rs9276162 0.882 0.280 6 32730680 downstream gene variant G/A snv 0.74 3
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs9276370
HLA-DQA2
0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 3
rs1383265 0.925 0.200 6 32772111 intergenic variant T/A;C snv 2
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs2647050 0.882 0.240 6 32701990 downstream gene variant T/C snv 0.36 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59