CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Disease: Basal cell carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs421284
rs421284
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease:
Basal cell carcinoma 		T 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs421284
rs421284
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease:
Basal cell carcinoma 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887 2016
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease:
Basal cell carcinoma 		C 0.700 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136 2015
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease:
Basal cell carcinoma 		C 0.700 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052 2014
dbSNP: rs401681
rs401681
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease:
Basal cell carcinoma 		C 0.700 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717 2009