Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs738409
rs738409
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.100 1.000 28 2011 2020
dbSNP: rs2281135
rs2281135
0.851 0.160 22 43936690 intron variant G/A snv 0.19
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2294918
rs2294918
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.010 1.000 1 2017 2017