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
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
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
CUI: C0011860
Disease: 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
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
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
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
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
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2016 2016
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 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
283 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
Gingival Recession
CUI: C0017572
Disease: Gingival Recession
1 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2016 2016
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