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.
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
478 0.851 0.120 2 233757013 intron variant T/A;G snv 0.700 1.000 1 2009 2009
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
535 0.851 0.120 2 233757013 intron variant T/A;G snv 0.700 1.000 1 2009 2009
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.120 2 233757013 intron variant T/A;G snv 0.700 1.000 1 2013 2013
Crigler Najjar syndrome, type 1
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
38 0.851 0.120 2 233757013 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.851 0.120 2 233757013 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Gilbert Disease (disorder)
CUI: C0017551
Disease: Gilbert Disease (disorder)
29 0.851 0.120 2 233757013 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.851 0.120 2 233757013 intron variant T/A;G snv 0.010 1.000 1 2017 2017
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.851 0.120 2 233757013 intron variant T/A;G snv 0.010 1.000 1 2017 2017