PON1, paraoxonase 1, 5444

N. diseases: 496; N. variants: 29
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11292716
rs11292716 		7 95305887 intron variant A/- delins
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2017 2017
dbSNP: rs1157745
rs1157745 		7 95311726 intron variant G/T snv 0.42
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2057681
rs2057681 		7 95308945 intron variant A/G snv 0.43
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2057681
rs2057681 		7 95308945 intron variant A/G snv 0.43
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		0.700 1.000 1 2012 2012
dbSNP: rs2237583
rs2237583 		7 95320865 intron variant C/G;T snv
CUI: C2257843
Disease: paraoxonase activity
paraoxonase activity 		0.700 1.000 1 2013 2013
dbSNP: rs3917481
rs3917481 		1.000 0.040 7 95321453 intron variant C/T snv 3.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3917502
rs3917502 		7 95316432 intron variant C/T snv 3.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3917510
rs3917510 		7 95313808 intron variant T/G snv 6.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3917532
rs3917532 		7 95310807 intron variant A/T snv 0.42
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3917539
rs3917539 		7 95308384 intron variant -/AA delins 0.42
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3917545
rs3917545 		7 95306923 intron variant A/C snv 0.13
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3917549
rs3917549 		7 95305887 intron variant A/- delins 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs854566
rs854566 		0.925 0.080 7 95319437 intron variant A/G snv 0.78
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs854566
rs854566 		0.925 0.080 7 95319437 intron variant A/G snv 0.78
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.100 0.889 27 1998 2019
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.100 0.864 22 1996 2018
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.100 0.938 16 1998 2018
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.100 0.929 14 2000 2019
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 1.000 12 1996 2019
dbSNP: rs854560
rs854560 		0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.100 1.000 12 2000 2019
dbSNP: rs854560
rs854560 		0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.100 0.909 11 2002 2017
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.090 0.667 9 2003 2014
dbSNP: rs854560
rs854560 		0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.080 1.000 8 2002 2017
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.070 0.857 7 2000 2010
dbSNP: rs662
rs662 		0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.070 1.000 7 2000 2020