Source: ALL

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
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C2677770
Disease: ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7
ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7 		0.700 0
dbSNP: rs4950928
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.090 0.889 9 2009 2019
dbSNP: rs4950928
rs4950928
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0242966
Disease: Systemic Inflammatory Response Syndrome
Systemic Inflammatory Response Syndrome 		0.010 1.000 1 2013 2013
dbSNP: rs4950928
rs4950928
CHI3L1
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
CHI3L1
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
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs4950928
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs4950928
rs4950928
CHI3L1
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
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
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
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 2019 2019