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.
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
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
Colonic Polyps
CUI: C0009376
Disease: Colonic Polyps
8 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2013 2013
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2012 2012
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2011 2011
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
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2013 2013
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
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
129 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2011 2011
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
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2013 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2011 2011
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
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
24 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2006 2006
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
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
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
Intraocular pressure disorder
CUI: C0595921
Disease: Intraocular pressure disorder
56 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2017 2017
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
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018