Variant: rs35897051 

    present in Gene: MPO
    present in Chromosome: 17
    Position on Chromosome: 58270865
    Alleles of this Variant: T/G

rs35897051 in MPO gene and Blood Protein Measurement PMID 30111768 2018 Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.

PMID 29875488 2018 Genomic atlas of the human plasma proteome.

rs35897051 in MPO gene and Myeloperoxidase Deficiency PMID 15108282 2004 Genetic characterization of myeloperoxidase deficiency in Italy.

PMID 6260268 1981 Hereditary myeloperoxidase deficiency.

PMID 9766845 1998 Clinical manifestation of myeloperoxidase deficiency.

rs35897051 in MPO gene and Myeloperoxidase Measurement PMID 23620142 2013 Gene-centric analyses in 8335 subjects of European ancestry additionally identified two rare MPO coding sequence variants that were associated with serum MPO levels (rs28730837, P = 5.21 × 10(-12); rs35897051, P = 3.32 × 10(-8)).