Disease: Primary biliary cirrhosis
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3