rs10468017, ALDH1A2

N. diseases: 12
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.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.890 0.900 10 2010 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 6 2009 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 2 2009 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 1 2011 2011
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 3 2009 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 2 2012 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 1 2011 2011
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 1 2012 2012
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
Drusen
CUI: C1260959
Disease: Drusen
18 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.010 1.000 1 2012 2012