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.
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2007 2007
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1 2009 2009
melanoma
CUI: C0025202
Disease: melanoma
515 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2006 2006
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
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
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
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
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
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
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1 2009 2009
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: 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
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
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 0.010 1.000 1 2004 2004
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
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
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)
CUI: C1847835
Disease: 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