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.
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
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
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2018 2018
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
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
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
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
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
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
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
Malignant neoplasm of colon and/or rectum
502 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019
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
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
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 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
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019
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
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
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
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
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
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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019