rs4775041, ALDH1A2

N. diseases: 8
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
1440 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 5 2008 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 3 2008 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 2 2012 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 3 2008 2013
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 3 2008 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 1 2011 2011
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 1 2011 2011
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 1 2008 2008