rs11568818, MMP7

N. diseases: 15
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.
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.720 0.750 4 2013 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.720 0.667 3 2013 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2016 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2012 2012
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2019 2019
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
63 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2013 2013
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2016 2016
Pancreatitis, Chronic
CUI: C0149521
Disease: Pancreatitis, Chronic
56 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2013 2013
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2017 2017
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 0.010 1.000 1 2015 2015