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.
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 1999 1999
Pterygium
CUI: C0033999
Disease: Pterygium
5 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2004 2004
Pterygium Of Conjunctiva And Cornea
CUI: C1867441
Disease: Pterygium Of Conjunctiva And Cornea
4 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2004 2004
Pterygium of eye
CUI: C4520843
Disease: Pterygium of eye
4 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2004 2004
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
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2005 2005
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2006 2006
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
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2006 2006
Tooth Loss
CUI: C0080233
Disease: Tooth Loss
8 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2006 2006
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
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2007 2009
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
81 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2007 2009
Stage 0 Gallbladder Cancer AJCC v8
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
56 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2007 2009
Stage IIA Gallbladder Cancer AJCC v8
CUI: C4525300
Disease: Stage IIA Gallbladder Cancer AJCC v8
56 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2007 2009