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: rs35724
rs35724
0.925 0.040 12 100561600 intron variant C/G snv 0.52
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs56163822
rs56163822
1.000 0.080 12 100493323 5 prime UTR variant G/T snv 4.7E-02 2.8E-02
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.010 1.000 1 2019 2019