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.
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
Germ cell tumor
CUI: C0205851
Disease: Germ cell tumor
5 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2005 2005
Small cell carcinoma of esophagus
CUI: C1112474
Disease: Small cell carcinoma of esophagus
5 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach stage IV
7 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2018 2018
Refractory anemias
CUI: C0002893
Disease: Refractory anemias
11 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1 2009 2009
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
Age-related cataract
CUI: C0036646
Disease: Age-related cataract
15 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2017 2017
Diabetic Polyneuropathies
CUI: C0271680
Disease: Diabetic Polyneuropathies
16 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2008 2008
Meningitis, Bacterial
CUI: C0085437
Disease: Meningitis, Bacterial
16 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2015 2015
Fuchs Endothelial Dystrophy
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
32 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2015 2015
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
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
AIDS related complex
CUI: C0001857
Disease: AIDS related complex
43 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2017 2017
Pelvic Organ Prolapse
CUI: C0877015
Disease: Pelvic Organ Prolapse
49 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
Oligospermia
CUI: C0028960
Disease: Oligospermia
72 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
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
Keratoconus
CUI: C0022578
Disease: Keratoconus
83 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
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 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
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1 2009 2009
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
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
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014