rs401681, CLPTM1L

N. diseases: 42
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.
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.730 0.750 4 2013 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.810 1.000 3 2009 2019
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2019 2019
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2019 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.800 1.000 17 2008 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.800 1.000 16 2008 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.100 1.000 15 2009 2018
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.740 1.000 7 2010 2018
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
CUI: C1832661
Disease: ANOPHTHALMIA AND PULMONARY HYPOPLASIA
80 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.100 1.000 11 2009 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.090 1.000 9 2009 2017
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.740 1.000 6 2009 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.050 0.800 5 2014 2017
Cleft palate with cleft lip
CUI: C0158646
Disease: Cleft palate with cleft lip
43 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.040 1.000 4 2013 2017
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.030 1.000 3 2011 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.020 1.000 2 2014 2017
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2017 2017
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.040 1.000 4 2013 2016
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.720 1.000 3 2010 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2016 2016
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.860 1.000 7 2010 2015
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.740 1.000 5 2010 2015
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 3 2009 2015
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 3 2009 2015