Variant: rs478093 

    present in Gene: PHGDH;LOC105378937
    present in Chromosome: 1
    Position on Chromosome: 119712503
    Alleles of this Variant: A/G

rs478093 in PHGDH;LOC105378937 gene and Glycine measurement PMID 31070104 2019 Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.

rs478093 in PHGDH;LOC105378937 gene and Insulin Sensitivity Measurement PMID 23378610 2013 Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.

rs478093 in PHGDH;LOC105378937 gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.