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.
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2013 2013
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2005 2005
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
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
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
Malignant mesothelioma
CUI: C0345967
Disease: Malignant mesothelioma
12 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2018 2018
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2011 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2015 2015
Panic Disorder
CUI: C0030319
Disease: Panic Disorder
101 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2015 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1 2012 2012
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
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.333 3 2003 2012
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
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
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
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 0.500 2 2007 2017
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.538 13 2005 2015
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
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
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2001 2019
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2001 2019
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
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.786 14 2001 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.800 15 2001 2017