Variant: rs750451693 

    present in Gene: CP
    present in Chromosome: 3
    Position on Chromosome: 149210191
    Alleles of this Variant: C/T

rs750451693 in CP gene and Movement Disorders PMID 14719552 2003 Aceruloplasminemia, an iron metabolic disorder.

PMID 18200628 2008 Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.

PMID 25089372 2015 Aceruloplasminaemia: a family with a novel mutation and long-term therapy with deferasirox.

PMID 16629161 2006 Molecular and pathological basis of aceruloplasminemia.