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.
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
Mixed type cataract
CUI: C1282365
Disease: Mixed type cataract
1 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2012 2012
Subfertility, Male
CUI: C0848676
Disease: Subfertility, Male
2 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
Varicocele
CUI: C0042341
Disease: Varicocele
3 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2018 2018
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
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
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
Stage IV Prostate Cancer AJCC v7
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
6 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2015 2015
Stage IV Prostate Cancer AJCC v8
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
6 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2015 2015
Stage IV Prostate Carcinoma
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
6 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2015 2015
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
Leukoplakia
CUI: C0023531
Disease: Leukoplakia
8 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2011 2011
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
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
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
Meningitis
CUI: C0025289
Disease: Meningitis
13 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2011 2011
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 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
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
Meningitis, Bacterial
CUI: C0085437
Disease: Meningitis, Bacterial
16 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2011 2015
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
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
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