Disorders

Apolipoprotein A-II Deficiency

Synonym(s): Familial Apolipoprotein A-II Deficiency due to APOA-II (Hiroshima)

Gene	Locus	Protein
APOA2	1q23.3	Apolipoprotein A-II

Laboratory	Test Method	Prenatal	Carrier *
Mayo Clinic - Minnesota, Molecular Genetics Laboratory - Rochester, MN, USA	• Sequence analysis of the entire coding region

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.