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.
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
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
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 stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.050 0.800 5 2009 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.050 0.800 5 2009 2014
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
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
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
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2014 2014
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
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
Malignant neoplasm of colon and/or rectum
502 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
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
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2015 2015
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 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
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
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