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
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
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.800 15 2001 2017
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.786 14 2001 2017
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
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2001 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.955 22 2002 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.955 22 2002 2018
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
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
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.070 0.857 7 2003 2015
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.070 0.857 7 2003 2015
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.040 0.500 4 2003 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.030 0.333 3 2003 2012
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
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 colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.100 0.538 13 2005 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