rs12483959, PNPLA3

N. diseases: 4
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 1.000 22 43930116 intron variant G/A;C;T snv 0.700 1.000 2 2011 2019
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 1.000 22 43930116 intron variant G/A;C;T snv 0.700 1.000 2 2011 2019
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 1.000 22 43930116 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 22 43930116 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011