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.
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
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
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
CUI: C0279626
Disease: 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
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
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
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
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
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
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
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
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
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
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
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