rs4823173, PNPLA3

N. diseases: 8
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
CUI: C0201836
Disease: Alanine aminotransferase measurement
77 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2019 2019
Aspartate aminotransferase measurement
CUI: C0201899
Disease: Aspartate aminotransferase measurement
76 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2019 2019
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2013 2013
Obesity
CUI: C0028754
Disease: Obesity
1111 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2015 2015
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2019 2019
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.020 1.000 2 2015 2018
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.010 1.000 1 2015 2015
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.010 1.000 1 2015 2015