rs3918242, MMP9

N. diseases: 54
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.
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2008 2008
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2009 2009
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2011 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2012 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 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
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.700 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.060 1.000 6 2013 2018
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 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
309 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2013 2017
Malignant neoplasm of urinary bladder
316 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 0.500 2 2013 2017
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
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2013 2013
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2013 2013
Paraseptal emphysema
CUI: C0264394
Disease: Paraseptal emphysema
3 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2013 2013
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2014 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2014 2014
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.060 1.000 6 2015 2020
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2015 2015
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2015 2015
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2015 2015
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
80 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2015 2015
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 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