rs174547, FADS2;FADS1

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.
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
19 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 2 2012 2016
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2012 2012
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 2 2011 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 2 2011 2016
RESTING HEART RATE
CUI: C1821417
Disease: RESTING HEART RATE
134 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 1 2010 2010
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2018 2018
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2011 2011
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.020 1.000 2 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2009 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.830 1.000 5 2011 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 3 2016 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 3 2009 2019