rs3918242, MMP9

N. diseases: 53
Source: BEFREE ×
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.060 1.000 6 2013 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
586 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.060 1.000 6 2015 2020
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
78 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2014 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
278 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2013 2017
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
290 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2013 2017
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
301 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2016 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2016 2017
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
289 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2013 2017
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2012 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2016 2018
Obesity
CUI: C0028754
Disease: Obesity
900 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2012 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2012 2017
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
157 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2011 2016
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
144 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
Asthma
CUI: C0004096
Disease: Asthma
714 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2019 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
233 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2016 2016
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
202 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2015 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2014 2014
Centriacinar Emphysema
CUI: C0221227
Disease: Centriacinar Emphysema
3 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
412 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2013 2013