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.
Prostate specific antigen measurement
95 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.800 1.000 1 2010 2010
Malignant Testicular Germ Cell Tumor
62 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 1 2010 2010
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
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
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1 2014 2014
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
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2009 2009
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2009 2009
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
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
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2014 2014
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 skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2011 2011
Nicotine Dependence
CUI: C0028043
Disease: Nicotine Dependence
178 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2014 2014
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2013 2013
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2014 2014
Squamous cell carcinoma of the head and neck
348 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.010 1.000 1 2010 2010
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
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.020 0.500 2 2013 2014
Squamous cell carcinoma of esophagus
329 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.020 0.500 2 2013 2014
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
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
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.710 0.667 3 2010 2014
Malignant neoplasm of urinary bladder
316 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.710 0.667 3 2010 2014
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