rs1052133, OGG1;CAMK1

N. diseases: 147
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.
Amyotrophic Lateral Sclerosis, Sporadic
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
90 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2007 2007
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
62 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2007 2007
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2007 2007
Hyperkeratosis
CUI: C0870082
Disease: Hyperkeratosis
19 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2007 2007
Keratosis
CUI: C0022593
Disease: Keratosis
10 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2007 2007
Melanosis
CUI: C0025209
Disease: Melanosis
23 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2007 2007
Melanosis coli
CUI: C0221391
Disease: Melanosis coli
5 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2007 2007
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2007 2007
Angiomyolipoma
CUI: C0206633
Disease: Angiomyolipoma
1 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2008 2008
Angiomyolipoma of kidney
CUI: C0241961
Disease: Angiomyolipoma of kidney
1 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2008 2008
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2008 2008
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.050 1.000 5 2009 2014
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2009 2009
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
50 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2009 2009
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2010 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2010 2013
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2010 2010
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2011 2019