rs17576, MMP9

N. diseases: 73
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.
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2015 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2015 2015
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2010 2010
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.020 0.500 2 2010 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.060 1.000 6 2009 2013
Asthma
CUI: C0004096
Disease: Asthma
1536 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.030 0.333 3 2005 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.020 0.500 2 2010 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2005 2005
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.030 0.667 3 2009 2013
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1 2018 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2005 2005
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2012 2012
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1 2018 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1 2016 2016
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2005 2005
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2015 2015
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2009 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2011 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.020 0.500 2 2012 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2017 2017
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2009 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2009 2009
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 0.010 1.000 1 2008 2008