rs2276109, MMP12

N. diseases: 18
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.
Forced expiratory volume function
CUI: C0016529
Disease: Forced expiratory volume function
1169 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.700 1.000 1 2015 2015
response to bronchodilator
CUI: C3548479
Disease: response to bronchodilator
1106 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.700 1.000 1 2015 2015
Asthma
CUI: C0004096
Disease: Asthma
1536 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.020 1.000 2 2009 2018
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.020 0.500 2 2017 2019
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2014 2014
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2013 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2013 2013
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1 2011 2011
Dementia
CUI: C0497327
Disease: Dementia
176 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1 2018 2018
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1 2011 2011
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2019 2019
Malignant neoplasm of urinary bladder
316 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2013 2013
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1 2018 2018
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1 2018 2018
Pulmonary Fibrosis
CUI: C0034069
Disease: Pulmonary Fibrosis
25 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2010 2010
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1 2018 2018
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 1.000 1 2010 2010