rs2896019, PNPLA3

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alanine aminotransferase measurement
77 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2010 2010
Aspartate aminotransferase measurement
76 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2010 2010
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2011 2011
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2018 2018
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2013 2013
Serum Alanine Aminotransferase Measurement
77 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2010 2010
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.710 1.000 2 2013 2014
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.710 1.000 2 2014 2018
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.710 1.000 2 2012 2018
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.810 1.000 3 2013 2018