ABCA1 Chromosome 9

ATP binding cassette subfamily A member 1
184 variants 184 Health Risk

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What This Gene Does
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in both alleles of this gene cause Tangier disease and familial high-density lipoprotein (HDL) deficiency. [provided by RefSeq, Sep 2019]
Gene Info
Gene Group
"ATP binding cassette subfamily A|ATPase phospholipid transporting"
Locus Type
gene with protein product
Location
9q31.1
Ensembl
ENSG00000165029
Associated Conditions (22)
Tangier disease
Hypoalphalipoproteinemia
primary
1
Hypertrophic cardiomyopathy
Cardiovascular phenotype
ABCA1-related disorder
Thymoma
Colon adenocarcinoma
Hypercholesterolemia
familial
Gastric cancer
Neurofibromatosis
type 1
Early-onset coronary artery disease
Colorectal cancer
Thyroid cancer
nonmedullary
variant
ABCA1-related dyslipidemia
+2 more conditions
Key Variants
All Variants (184)
RSID Category Clinical Significance Conditions
RS200532064 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS200572505 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS200788099 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS200831433 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS200928212 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS201076284 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS201134913 Health Risk Conflicting classifications of pathogenicity
RS201555773 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS201599169 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS2066718 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS35819696 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS368288959 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS368667473 Health Risk Conflicting classifications of pathogenicity
RS369476391 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS371136175 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS371949943 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS372207376 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS374418354 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS375234343 Health Risk Conflicting classifications of pathogenicity
RS376321182 Health Risk Conflicting classifications of pathogenicity
RS377248142 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS377600690 Health Risk Conflicting classifications of pathogenicity
RS377673145 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS528656411 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS535255845 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS536848431 Health Risk Conflicting classifications of pathogenicity
RS537176920 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS538614702 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS539279965 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS539455164 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS547220092 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS547281385 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS548468204 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS550787183 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS551547276 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS551884479 Health Risk Conflicting classifications of pathogenicity
RS557173577 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS557529420 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS563149622 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS564049659 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS564764153 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS569604699 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS572043133 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS572405590 Health Risk Conflicting classifications of pathogenicity ABCA1-related disorder, ABCA1-related disorder
RS748663329 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS751669145 Health Risk Conflicting classifications of pathogenicity Tangier disease, Hypoalphalipoproteinemia, primary
RS752051518 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS752528416 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
RS752583258 Health Risk Conflicting classifications of pathogenicity
RS753324965 Health Risk Conflicting classifications of pathogenicity Hypoalphalipoproteinemia, primary, 1
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