SLC27A5, solute carrier family 27 member 5, 10998

N. diseases: 111; N. variants: 6
Disease: Polysomnography ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs58632700
rs58632700
Entrez Id: 10998;55663;112268251
Gene Symbol: SLC27A5;ZNF446;LOC112268251
SLC27A5;ZNF446;LOC112268251
CUI: C0162701
Disease:
Polysomnography 		A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012