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.
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
225 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.850 1.000 8 2010 2018
melanoma
CUI: C0025202
Disease: melanoma
389 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.850 1.000 6 2011 2016
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.840 1.000 6 2008 2014
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
56 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.800 3 2009 2016
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
165 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.800 2 2010 2014
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
183 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.800 2 2010 2017
Prostate specific antigen measurement
89 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.800 1 2011 2011
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.700 1 2009 2009
Carcinoma testes
CUI: C0677483
Disease: Carcinoma testes
79 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.700 1 2010 2010
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
136 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.050 1.000 5 2013 2016
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
409 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.040 1.000 4 2013 2014
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
400 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.040 1.000 4 2013 2014
Cleft palate with cleft lip
CUI: C0158646
Disease: Cleft palate with cleft lip
2 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.030 1.000 3 2013 2016
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
224 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.030 1.000 3 2011 2014
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
67 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.020 1.000 2 2014 2014
Experimental Organism Basal Cell Carcinoma
33 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.020 1.000 2 2011 2013
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
60 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.020 1.000 2 2014 2016
Squamous cell carcinoma of esophagus
148 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.020 0.500 2 2014 2015
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
154 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.010 1.000 1 2015 2015
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
23 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.010 1.000 1 2011 2011
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.010 1.000 1 2015 2015
Squamous cell carcinoma of the head and neck
288 0.679 0.464 5 1321972 intron variant C/T snp 0.48 0.010 1.000 1 2010 2010