rs1052133, CAMK1;OGG1

N. diseases: 77
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.
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
228 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2000 2000
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
223 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2001 2001
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
60 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2001 2001
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
66 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2001 2001
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
61 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2005 2005
cervical cancer
CUI: C4048328
Disease: cervical cancer
87 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2005 2005
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
100 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2005 2005
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
79 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2005 2005
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.030 1.000 3 2002 2006
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
67 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2006 2006
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
11 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1 2006 2006
Adenoma
CUI: C0001430
Disease: Adenoma
73 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.020 0.500 2 2005 2007
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
58 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1 2007 2007
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
65 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1 2007 2007
Hyperkeratosis
CUI: C0870082
Disease: Hyperkeratosis
11 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2007 2007
Keratosis
CUI: C0022593
Disease: Keratosis
7 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2007 2007
Melanosis
CUI: C0025209
Disease: Melanosis
4 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2007 2007
Melanosis coli
CUI: C0221391
Disease: Melanosis coli
4 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2007 2007
Angiomyolipoma
CUI: C0206633
Disease: Angiomyolipoma
1 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2008 2008
Angiomyolipoma of kidney
CUI: C0241961
Disease: Angiomyolipoma of kidney
1 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2008 2008
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
51 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.020 1.000 2 2007 2009
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
41 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.020 1.000 2 2007 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2009 2009
Secondary malignant neoplasm of lymph node
66 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2009 2009
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
68 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 0.010 1.000 1 2010 2010