Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7793921
rs7793921
Entrez Id: 908;5723
Gene Symbol: CCT6A;PSPH
CCT6A;PSPH
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