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ACADVL rs1057516818: what the research says

rs1057516818
Trait
Moderate evidenceGene: ACADVL

This SNP is located in the ACADVL gene region and is noted as a common variant in clinical databases.

Common

Our full long-form research profile for rs1057516818 — genotype interpretations, evidence review, and FAQ — is being written and will appear on this page soon.
dbSNP ClinVar GWAS Catalog Google Scholar

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Related variants in ACADVL

rs140629318
ACADVL
Carrier Status
Moderate

This variant is associated with carrier status for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) deficiency, an autosomal recessive metabolic disorder.

rs200788251
ACADVL
Carrier Status
Moderate

This variant is associated with carrier status for Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency.

rs118204017
ACADVL
Carrier Status
Moderate

This variant is associated with carrier status for VLCAD deficiency.