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: rs402710
rs402710
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE <i>CLPTM1L</i> gene rs402710 (C > T) and rs401681 (C > T) polymorphisms associate with decreased cancer risk: a meta-analysis. 29254260 2017
dbSNP: rs402710
rs402710
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE Increased cancer risk was found between TERT-rs2736100, as well as CLPTM1L-rs402710 and cancer susceptibility. 23707794 2013