rs1883025, ABCA1

N. diseases: 13
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.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 12 2009 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 5 2010 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 1 2012 2012
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.740 0.600 5 2011 2018
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 5 2009 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2019 2019
Drusen
CUI: C1260959
Disease: Drusen
18 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.010 1.000 1 2012 2012
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.010 1 2014 2014
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.010 1 2014 2014