CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
T 0.740 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer. 29422604 2018
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
0.740 GeneticVariation BEFREE This meta-analysis suggests that T allele of CLPTM1L-telomerase reverse transcriptase rs401681 polymorphism is associated with an increased PC risk, especially among Chinese. 25284078 2015
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
0.740 GeneticVariation BEFREE A small number of common susceptibility loci have been identified for pancreatic cancer, one of which is marked by rs401681 in the TERT-CLPTM1L gene region on chromosome 5p15.33. 25940397 2015
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
0.740 GeneticVariation GWASCAT Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. 26098869 2015
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
0.740 GeneticVariation BEFREE Our data suggests that the T allele of rs401681 in CLPTM1L-TERT locus predisposes its carriers to pancreatic cancer, and further research into the function of CLPTM1L-TERT locus and its potential biological mechanism association may be warranted. 24577890 2014
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
0.740 GeneticVariation BEFREE These findings suggested that rs401681 C allele was a low-penetrance risk allele for the development of cancers of lung, bladder, prostate and basal cell carcinoma, but a potential protective allele for melanoma and pancreatic cancer. 23226346 2012
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease:
Pancreatic carcinoma
T 0.740 GeneticVariation GWASCAT A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. 20101243 2010