rs646776, CELSR2

N. diseases: 25
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.
Low density lipoprotein cholesterol measurement
1142 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 12 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 8 2009 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.830 1.000 7 2011 2016
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 6 2008 2013
High density lipoprotein measurement
1440 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.800 1.000 4 2012 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.720 1.000 3 2014 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.810 1.000 2 2009 2012
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2013 2013
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2014 2014
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2018 2018
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2016 2016
Carotid Artery Diseases
CUI: C0007273
Disease: Carotid Artery Diseases
6 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2009 2009
Catalase measurement
CUI: C0523550
Disease: Catalase measurement
2 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2017 2017
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2015 2015
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2010 2010
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2009 2009
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2013 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2013 2013
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2018 2018
Premature coronary artery atherosclerosis
43 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2019 2019
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2012 2012