rs1800588, ALDH1A2;LIPC

N. diseases: 16
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 6 2012 2019
High density lipoprotein measurement
1440 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 5 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 4 2012 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.030 1.000 3 2009 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.720 1.000 3 2009 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.020 1.000 2 2009 2013
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.700 1.000 2 2008 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2017 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2017 2017
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2014 2014
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1 2018 2018
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2013 2013
Obesity
CUI: C0028754
Disease: Obesity
1111 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2017 2017
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.700 1.000 1 2012 2012
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.010 1.000 1 2015 2015