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.
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2005 2019
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Cervical Squamous Cell Carcinoma
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
44 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2005 2019
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
Childhood Hepatocellular Carcinoma
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
17 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2015 2015
Childhood Kidney Wilms Tumor
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
36 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
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
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.040 0.500 4 2003 2013
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.500 18 2005 2019
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 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
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
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
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 0.500 2 2011 2012
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
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2001 2019