rs4950928, CHI3L1

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.
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
CUI: C2677770
Disease: ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
1 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.700 0
Asthma
CUI: C0004096
Disease: Asthma
1536 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.090 0.889 9 2009 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.040 1.000 4 2009 2012
Allergic asthma
CUI: C0155877
Disease: Allergic asthma
55 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2009 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2019 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2019 2019
Bronchial Hyperreactivity
CUI: C0085129
Disease: Bronchial Hyperreactivity
18 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2009 2009
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2016 2016
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2011 2011
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1 2009 2009
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2012 2012
IgE-mediated allergic asthma
CUI: C1827849
Disease: IgE-mediated allergic asthma
46 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2009 2009
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2017 2017
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2012 2012
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2019 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2015 2015
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2019 2019
Mitral Valve Stenosis
CUI: C0026269
Disease: Mitral Valve Stenosis
7 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2012 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2012 2012
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 0.010 1.000 1 2015 2015