Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72549398
ABCB11
0.790 0.240 2 168932442 missense variant G/A snv 1.2E-05 7.0E-06 8
rs2109505
ABCB4
0.851 0.200 7 87450090 splice region variant T/A snv 0.21 0.22 6
rs11568372
ABCB11
0.827 0.240 2 168990819 missense variant T/C snv 2.5E-04 1.1E-04 5
rs113090017
NR1H4
0.882 0.200 12 100532538 stop gained C/A;G;T snv 4.0E-06; 2.4E-05 4
rs111033609
ATP8B1
0.882 0.200 18 57695188 missense variant C/A;T snv 4.0E-06 3
rs121909100
LOC100505549 ; ATP8B1
0.882 0.200 18 57669433 missense variant A/G snv 9.6E-05 9.1E-05 3
rs121909101
ATP8B1
0.925 0.200 18 57674993 missense variant C/T snv 2
rs515726137
LOC100505549 ; ATP8B1
1.000 0.200 18 57669422 stop gained C/A snv 1.4E-05 2
rs879255644
NR1H4
0.925 0.200 12 100511115 inframe insertion -/AAA delins 2
rs515726138
ATP8B1
1.000 0.200 18 57697797 missense variant G/T snv 8.0E-06 1