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.
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
Diseases of mitral valve
CUI: C0026265
Disease: Diseases of mitral valve
2 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2017 2017
Rheumatic disease of mitral valve
CUI: C0264765
Disease: Rheumatic disease of mitral valve
2 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2017 2017
Spider nevus
CUI: C0085666
Disease: Spider nevus
2 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
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
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
Endometriosis of uterus
CUI: C0341858
Disease: Endometriosis of uterus
4 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2018 2018
Mitral Valve Stenosis
CUI: C0026269
Disease: Mitral Valve Stenosis
7 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019
Hantavirus Infections
CUI: C0242994
Disease: Hantavirus Infections
10 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
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
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
Large-artery atherosclerosis (embolus/thrombosis)
35 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2020 2020
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019
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
Malignant neoplasm of gastrointestinal tract
55 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
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
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
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
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
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
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
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2017 2017
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
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