APOA1

apolipoprotein A1
OMIM: 107680, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green APOA1 in Mendeliome Version 2.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Amyloidosis, hereditary systemic 3, MIM# 620657 Amyloidosis, 3 or more types MIM#105200 Hypoalphalipoproteinemia, primary, 2 MIM#618463 Hypoalphalipoproteinemia, primary, 2, intermediate MIM#619836
Green APOA1 in Amyloidosis Version 2.0	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Green Expert list Phenotypes Amyloidosis, 3 or more types, MIM#105200
Green APOA1 in Dyslipidaemia Level 2: Endocrine disorders; Cardiovascular disorders Version 1.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Hypoalphalipoproteinaemia, primary, 2, intermediate, MIM# 619836
Green APOA1 in Hereditary Neuropathy Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes Amyloidosis, 3 or more types 105200 Renal failure, Axonal sensory-motor neuropathy, amyloid nephropathy
Green APOA1 in Transplant Co-Morbidity Level 2: Screening Version 1.0	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Hypoalphalipoproteinaemia, primary, 2, intermediate, MIM# 619836