CHI3L1, chitinase 3 like 1, 1116

N. diseases: 420; N. variants: 9
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: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0023895
Disease: Liver diseases
Liver diseases
Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity
Respiratory Tract Diseases 0.010 1.000 1 2009 2009
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0037090
Disease: Signs and Symptoms, Respiratory
Signs and Symptoms, Respiratory
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
Digestive System Diseases; Infections 0.010 1.000 1 2012 2012
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2009 2009
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff
Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2016 2016
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
Systemic Inflammatory Response Syndrome
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2013 2013
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2017 2017
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2019 2019