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.
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2005 2019
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2005 2019
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2005 2019
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.070 1.000 7 2006 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.050 1.000 5 2006 2019
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.050 1.000 5 2006 2013
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.040 1.000 4 2006 2018
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
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
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
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.070 0.857 7 2007 2014
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
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
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
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
Stage IIB Gallbladder Cancer AJCC v8
CUI: C4525301
Disease: Stage IIB 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 III Gallbladder Cancer AJCC v8
CUI: C4525302
Disease: Stage III 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 IV Gallbladder Cancer AJCC v8
CUI: C4525305
Disease: Stage IV 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