Disease: Serum Alanine Aminotransferase Measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2078087
rs2078087
Entrez Id: 23057
Gene Symbol: NMNAT2
NMNAT2
CUI: C1883008
Disease:
Serum Alanine Aminotransferase Measurement 		A 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012