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: C0596263
Disease:
Carcinogenesis
0.010 GeneticVariation BEFREE These results suggested that the rs401681 polymorphism contributes to lung carcinogenesis only in patients harboring an EGFR mutation. 29033187 2017