CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Disease: Bronchial Obstruction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs31489
rs31489
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0221725
Disease:
Bronchial Obstruction 		0.010 GeneticVariation BEFREE The rs31489 variant on 5p15.33 is associated with bronchial obstruction, presence and severity of emphysema, and lung cancer. 21622582 2011