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.
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
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
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
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
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.700 1.000 3 2009 2015
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
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
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
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
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
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
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
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
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
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
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 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
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
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 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
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