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: C0155877
Disease: Allergic asthma
Allergic asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10399931
rs10399931
0.807 0.320 1 203186952 upstream gene variant T/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 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: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 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: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.090 0.889 9 2009 2019
dbSNP: rs10399931
rs10399931
0.807 0.320 1 203186952 upstream gene variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.030 1.000 3 2009 2019
dbSNP: rs10399805
rs10399805
0.851 0.240 1 203186870 upstream gene variant G/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12141494
rs12141494
1.000 0.080 1 203182297 intron variant G/A snv 0.41
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1538372
rs1538372
1.000 0.080 1 203185404 intron variant A/G snv 0.65 0.67
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System 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
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
0.700 0
dbSNP: rs10399805
rs10399805
0.851 0.240 1 203186870 upstream gene variant G/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs10920578
rs10920578
1 203184966 intron variant C/T snv 0.40
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs903357
rs903357
1 203178482 upstream gene variant G/A snv 0.40
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
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: 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: 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
CUI: C0699790
Disease: Colon Carcinoma
Colon 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: 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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10399931
rs10399931
0.807 0.320 1 203186952 upstream gene variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs880633
rs880633
0.925 0.160 1 203183673 missense variant T/C snv 0.45 0.41
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs10399931
rs10399931
0.807 0.320 1 203186952 upstream gene variant T/A;C 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
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: 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
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
Immune System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10399805
rs10399805
0.851 0.240 1 203186870 upstream gene variant G/A;T snv
CUI: C0677898
Disease: invasive cancer
invasive cancer
Neoplasms 0.010 1.000 1 2014 2014