CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma
Neoplasms 0.860 1.000 7 2010 2015
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
Neoplasms 0.810 1.000 3 2009 2019
dbSNP: rs31489
rs31489
0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
Neoplasms 0.810 1.000 2 2009 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.800 1.000 17 2008 2018
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.800 1.000 16 2008 2018
dbSNP: rs31490
rs31490
0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2014 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
Prostate specific antigen measurement
0.800 1.000 1 2010 2010
dbSNP: rs31489
rs31489
0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.750 1.000 7 2008 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.740 1.000 7 2010 2018
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
Neoplasms 0.740 1.000 6 2009 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.740 1.000 5 2010 2015
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.730 0.750 4 2013 2019
dbSNP: rs31489
rs31489
0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.720 1.000 3 2010 2017
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.720 1.000 3 2010 2016
dbSNP: rs380286
rs380286
0.776 0.200 5 1320132 intron variant G/A snv 0.47
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.710 1.000 3 2014 2019
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.710 0.667 3 2010 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.710 0.667 3 2010 2014
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
Neoplasms 0.700 1.000 3 2009 2015
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm
Neoplasms 0.700 1.000 3 2009 2015
dbSNP: rs401681
rs401681
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
Neoplasms 0.700 1.000 3 2009 2015
dbSNP: rs421284
rs421284
0.882 0.040 5 1325475 non coding transcript exon variant T/C;G snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm
Neoplasms 0.700 1.000 2 2016 2019
dbSNP: rs421284
rs421284
0.882 0.040 5 1325475 non coding transcript exon variant T/C;G snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma
Neoplasms 0.700 1.000 2 2016 2019
dbSNP: rs421284
rs421284
0.882 0.040 5 1325475 non coding transcript exon variant T/C;G snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer
Neoplasms 0.700 1.000 2 2016 2019
dbSNP: rs10462706
rs10462706
0.827 0.080 5 1343679 intron variant C/T snv 0.14
Malignant neoplasm of other sites within the lip and oral cavity
Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
0.827 0.080 5 1343679 intron variant C/T snv 0.14
Malignant neoplasm of lateral floor of mouth
Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016