MMP9, matrix metallopeptidase 9, 4318

N. diseases: 1337; N. variants: 31
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: rs3918241
rs3918241 		0.925 0.080 20 46007096 upstream gene variant T/A snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3918241
rs3918241 		0.925 0.080 20 46007096 upstream gene variant T/A snv 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3918241
rs3918241 		0.925 0.080 20 46007096 upstream gene variant T/A snv 0.14
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.060 1.000 6 2015 2020
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.060 1.000 6 2013 2018
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.020 1.000 2 2012 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.020 0.500 2 2011 2016
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.020 1.000 2 2012 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2016 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 0.500 2 2013 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.020 1.000 2 2016 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 0.500 2 2013 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		Cardiovascular Diseases 0.020 1.000 2 2014 2019
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2016 2018
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 1.000 2 2012 2015
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.020 1.000 2 2016 2016
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 0.500 2 2013 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0264394
Disease: Paraseptal emphysema
Paraseptal emphysema 		Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0026265
Disease: Diseases of mitral valve
Diseases of mitral valve 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0264765
Disease: Rheumatic disease of mitral valve
Rheumatic disease of mitral valve 		0.010 1.000 1 2017 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 < 0.001 1 2017 2017
dbSNP: rs3918242
rs3918242 		0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2019 2019