rs10455872, LPA

N. diseases: 33
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.830 1.000 6 2011 2018
Aortic valve calcification
CUI: C0428791
Disease: Aortic valve calcification
4 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.820 1.000 2 2013 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.800 1.000 6 2012 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.800 1.000 4 2012 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.770 0.875 8 2012 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.710 1.000 2 2013 2015
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 2 2012 2012
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2017 2017
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2014 2014
response to statin
CUI: C3549252
Disease: response to statin
8 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2012 2012
Rheumatic aortic stenosis
CUI: C0155567
Disease: Rheumatic aortic stenosis
5 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2018 2018
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.700 1.000 1 2012 2012
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.040 1.000 4 2012 2019
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
19 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.030 1.000 3 2014 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.030 0.333 3 2013 2017
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2013 2013
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2012 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2012 2012
Calcific stenosis
CUI: C0333184
Disease: Calcific stenosis
4 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2014 2014
Calcification of mitral valve
CUI: C0919718
Disease: Calcification of mitral valve
2 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2016 2016
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2019 2019
Chronic myocardial ischemia
CUI: C0264694
Disease: Chronic myocardial ischemia
7 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2019 2019
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2019 2019
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2017 2017