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.
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
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
Malignant Testicular Germ Cell Tumor
CUI: C0855197
Disease: 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
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
Prostate specific antigen measurement
CUI: C0201544
Disease: 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
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
CUI: C1168401
Disease: 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