Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease 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
Diabetes Mellitus, Non-Insulin-Dependent
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: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
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: C0085129
Disease: Bronchial Hyperreactivity
Bronchial Hyperreactivity
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: C0155877
Disease: Allergic asthma
Allergic asthma
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: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
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: C0036202
Disease: Sarcoidosis
Sarcoidosis
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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
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: C0036341
Disease: Schizophrenia
Schizophrenia
0.040 1.000 4 2009 2012
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
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: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
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: C0026269
Disease: Mitral Valve Stenosis
Mitral Valve Stenosis
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: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff
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: C0023895
Disease: Liver diseases
Liver 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
Systemic Inflammatory Response Syndrome
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: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial 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: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
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: C0006826
Disease: Malignant Neoplasms
Malignant 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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
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: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
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: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
Malignant neoplasm of colon and/or rectum
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
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: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
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: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
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: C0037090
Disease: Signs and Symptoms, Respiratory
Signs and Symptoms, Respiratory
0.010 1.000 1 2017 2017