CCL11, C-C motif chemokine ligand 11, 6356

N. diseases: 250; N. variants: 7
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: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.030 0.667 3 2004 2006
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.020 1.000 2 2012 2015
dbSNP: rs4795895
rs4795895 		1.000 0.120 17 34284427 upstream gene variant A/G snv 0.86
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.020 1.000 2 2012 2017
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 < 0.001 1 2004 2004
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0340288
Disease: Stable angina
Stable angina 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0917801
Disease: Sleeplessness
Sleeplessness 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C3272265
Disease: Three Vessel Coronary Disease
Three Vessel Coronary Disease 		0.010 < 0.001 1 2015 2015
dbSNP: rs1129844
rs1129844 		0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1411351750
rs1411351750 		1.000 0.080 17 34285859 synonymous variant C/T snv 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 < 0.001 1 2007 2007
dbSNP: rs17735961
rs17735961 		1.000 0.040 17 34285321 upstream gene variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs17809012
rs17809012 		0.925 0.160 17 34285425 upstream gene variant A/G;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs17809012
rs17809012 		0.925 0.160 17 34285425 upstream gene variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs17809012
rs17809012 		0.925 0.160 17 34285425 upstream gene variant A/G;T snv
CUI: C3178801
Disease: Stroke, Lacunar
Stroke, Lacunar 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs17809012
rs17809012 		0.925 0.160 17 34285425 upstream gene variant A/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1860184
rs1860184 		1.000 0.120 17 34286113 intron variant A/C;T snv
CUI: C3178801
Disease: Stroke, Lacunar
Stroke, Lacunar 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4795895
rs4795895 		1.000 0.120 17 34284427 upstream gene variant A/G snv 0.86
CUI: C3178801
Disease: Stroke, Lacunar
Stroke, Lacunar 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4795896
rs4795896 		1.000 0.040 17 34285233 upstream gene variant T/C snv 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018