rs74913549, PANX1

N. diseases: 3
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 11 94180526 intron variant T/A;C snv 0.700 1.000 1 2018 2018
Aspartate aminotransferase measurement
CUI: C0201899
Disease: Aspartate aminotransferase measurement
76 11 94180526 intron variant T/A;C snv 0.700 1.000 1 2018 2018
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 11 94180526 intron variant T/A;C snv 0.700 1.000 1 2018 2018