ACADVL · rs28934585
Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 2,466 Black/admixed ancestry individuals; replicated in up to 1,653 European, Hispanic, Asian or Black individuals.
The effect Each copy of the T allele shifted the measure 0.352 lower (95% confidence interval 0.26-0.45); p = 3 × 10−13.
Where it sits Chromosome 17, band 17p13.1 — a missense change in ACADVL.
What ClinVar records
Classification
Benign for Very long chain acyl-CoA dehydrogenase deficiency; reviewed by expert panel (3 of 4 stars, 12 submitters), last evaluated 2022-03-08.
ClinVar record 38798 NM_000018.4(ACADVL):c.194C>T (p.Pro65Leu)
What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
rs28934585 is a single position in the genome, in or near the ACADVL gene. Published research associates it with carnitine c12 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
GWAS Catalog, Nature communications 2022, PMID:35995766. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Carnitine C12 levels (rs28934585). MyGeneLog™. https://www.mygenelog.com/variants/rs28934585