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
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
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.050 1.000 5 2002 2012
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
Adult Hepatocellular Carcinoma
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
14 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2015 2015
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2012 2012
Age-related cataract
CUI: C0036646
Disease: Age-related cataract
15 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2012 2018
AIDS related complex
CUI: C0001857
Disease: AIDS related complex
43 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2017 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.060 1.000 6 2007 2019
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
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
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2010 2010
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.070 0.857 7 2007 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.944 18 2002 2019
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2015 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.040 1.000 4 2005 2019
Carcinoma in situ of uterine cervix
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
18 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.070 0.857 7 2007 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.967 30 1999 2019
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2011 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2012 2016