SLC7A2, solute carrier family 7 member 2, 6542

N. diseases: 30; N. variants: 4
Disease: Amino acids measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56335308
rs56335308
Entrez Id: 6542
Gene Symbol: SLC7A2
SLC7A2
CUI: C0201874
Disease:
Amino acids measurement 		G 0.700 GeneticVariation GWASCAT Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. 30659259 2019