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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2016 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.020 1.000 2 2016 2018
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
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
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
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2018 2018
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
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
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: 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
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
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 0.010 1.000 1 2019 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: 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
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