Disease: Primary biliary cirrhosis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs6974491
ELMO1
0.807 0.120 7 37334906 intron variant G/A snv 0.14 2