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.
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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.967 30 1999 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.967 30 1999 2019
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.500 18 2005 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.944 18 2002 2019
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
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
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
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
Childhood Acute Lymphoblastic Leukemia
261 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2011 2019
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2001 2019
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2001 2019
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.667 3 2001 2019
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
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
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Cervical Squamous Cell Carcinoma
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
44 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.010 1.000 1 2019 2019