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.
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.827 0.160 2 233719115 missense variant G/C snv 2.4E-05 2.1E-05 0.020 1.000 2 2006 2016
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.827 0.160 2 233719115 missense variant G/C snv 2.4E-05 2.1E-05 0.010 1.000 1 2008 2008
Crigler Najjar syndrome, type 2
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
27 0.827 0.160 2 233719115 missense variant G/C snv 2.4E-05 2.1E-05 0.010 1.000 1 2007 2007
Gilbert Disease (disorder)
CUI: C0017551
Disease: Gilbert Disease (disorder)
29 0.827 0.160 2 233719115 missense variant G/C snv 2.4E-05 2.1E-05 0.010 1.000 1 2007 2007
Hyperbilirubinemia, Neonatal
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
15 0.827 0.160 2 233719115 missense variant G/C snv 2.4E-05 2.1E-05 0.010 1.000 1 2011 2011