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: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2012 2012
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2012 2012
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2012 2012
dbSNP: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.020 0.500 2 2013 2014
dbSNP: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.020 0.500 2 2013 2014
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.020 0.500 2 2009 2013
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
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
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: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.730 0.750 4 2013 2019
dbSNP: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.050 0.800 5 2014 2017
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: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.100 1.000 15 2009 2018
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.100 1.000 13 2009 2018
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.100 1.000 13 2009 2018
dbSNP: rs402710
rs402710 		0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.100 1.000 13 2009 2018
dbSNP: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.100 1.000 11 2009 2017
dbSNP: rs401681
rs401681 		0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.090 1.000 9 2009 2017
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: 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: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		Neoplasms 0.740 1.000 6 2009 2017
dbSNP: rs31489
rs31489 		0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.050 1.000 5 2010 2014
dbSNP: rs31489
rs31489 		0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.050 1.000 5 2010 2014