Disease: Primary biliary cirrhosis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2313430
IKZF3
0.925 0.160 17 39773563 intron variant T/C snv 0.48 2
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs9909593
IKZF3
0.925 0.160 17 39813896 intron variant A/G snv 0.38 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs3816470
IKZF3
0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs11557466
ZPBP2
0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 3
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs9907088 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 3
rs9904624 0.925 0.160 17 39880333 downstream gene variant A/G snv 0.39 2
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2305479
GSDMB
0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3