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 measurement
CUI: C0344395
Disease: Bilirubin measurement
535 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.800 1.000 6 2009 2015
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
478 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.700 1.000 4 2009 2013
HIV Infections
CUI: C0019693
Disease: HIV Infections
142 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.700 1.000 1 2015 2015
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.700 1.000 1 2013 2013
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
3 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.700 0
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.020 1.000 2 2010 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.020 0.500 2 2017 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2017 2017
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
62 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2010 2010
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2015 2015
Gilbert Disease (disorder)
CUI: C0017551
Disease: Gilbert Disease (disorder)
29 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2010 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2013 2013
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.807 0.240 2 233763993 intron variant G/T snv 0.36 0.010 1.000 1 2013 2013