Disease: Hepatitis B
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs3130215
COL11A2P1
0.882 0.240 6 33107186 intron variant A/G snv 0.69 3
rs423639 0.882 0.240 6 33019997 intergenic variant C/T snv 0.11 3
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs11752643 0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02 2
rs154972 0.925 0.120 6 32932874 downstream gene variant A/G snv 0.35 2