CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Disease: Lower Urinary Tract Symptoms ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs381949
rs381949
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0574785
Disease:
Lower Urinary Tract Symptoms 		G 0.700 GeneticVariation GWASCAT Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. 30410027 2018