Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs31489
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.810 1.000 1 2009 2014
dbSNP: rs31489
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.740 1.000 3 2010 2018
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 3 2009 2015
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 3 2009 2015
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 3 2009 2015
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.710 0.667 2 2010 2014
dbSNP: rs10462706
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14
CUI: C0496758
Disease: Malignant neoplasm of lateral floor of mouth
Malignant neoplasm of lateral floor of mouth 		0.700 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14
CUI: C0153407
Disease: Malignant neoplasm of other sites within the lip and oral cavity
Malignant neoplasm of other sites within the lip and oral cavity 		0.700 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14
CUI: C0153380
Disease: Malignant neoplasm of other specified parts of mouth
Malignant neoplasm of other specified parts of mouth 		0.700 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.700 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14
CUI: C0153369
Disease: Malignant neoplasm of anterior portion of floor of mouth
Malignant neoplasm of anterior portion of floor of mouth 		0.700 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14
CUI: C0153368
Disease: Malignant neoplasm of floor of mouth
Malignant neoplasm of floor of mouth 		0.700 1.000 1 2016 2016
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.800 1.000 1 2010 2010
dbSNP: rs401681
rs401681
CLPTM1L
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 		0.730 0.750 1 2013 2019
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma 		0.860 1.000 1 2010 2015
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.800 1.000 1 2008 2018
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.810 1.000 1 2009 2019
dbSNP: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs380286
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.710 1.000 2 2014 2019
dbSNP: rs380286
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47
CUI: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		0.700 1.000 1 2018 2018
dbSNP: rs380286
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2019 2019
dbSNP: rs380286
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47
CUI: C0153535
Disease: Malignant melanoma of skin of upper limb
Malignant melanoma of skin of upper limb 		0.700 1.000 1 2018 2018
dbSNP: rs380286
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.700 1.000 1 2018 2018
dbSNP: rs381949
rs381949
CLPTM1L
1.000 0.040 5 1322353 intron variant G/A snv 0.44
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		0.700 1.000 1 2018 2018