rs1136410, PARP1

N. diseases: 70
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.030 0.667 3 2010 2014
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2010 2010
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2010 2010
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2010 2010
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2010 2010
Meningitis
CUI: C0025289
Disease: Meningitis
13 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2011 2011
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2011 2011
Secondary malignant neoplasm of lymph node
188 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2011 2011
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2011 2011
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.030 1.000 3 2012 2017
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.030 1.000 3 2012 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.020 1.000 2 2012 2017
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.020 1.000 2 2012 2018
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.020 1.000 2 2012 2018
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.020 1.000 2 2012 2018
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2012 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2012 2012
Triple vessel disease
CUI: C0856738
Disease: Triple vessel disease
3 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2012 2012
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.020 1.000 2 2013 2017
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.020 1.000 2 2013 2017
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2013 2013
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2013 2013
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2013 2013
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.030 1.000 3 2014 2019
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014