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.
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
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
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
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
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
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
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
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
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
CUI: C0005684
Disease: 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
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
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
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
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
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
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.620 0.640 5 1321972 intron variant C/T snv 0.48 0.030 1.000 3 2011 2014
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
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