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Succinic acid/Methylmalonic acid levels

SDHA · rs151266052

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 1.02 higher (95% confidence interval 0.72-1.32); p = 4 × 10−11.

Where it sits Chromosome 5, band 5p15.33 — a missense change in SDHA.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Succinic acid/Methylmalonic acid levels — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Succinic acid/Methylmalonic acid levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Succinic acid/Methylmalonic acid levels compared to the general population.
Source

Questions about rs151266052

What is rs151266052?

rs151266052 is a single position in the genome, in or near the SDHA gene. Published research associates it with succinic acid/methylmalonic acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs151266052 mean I will get this?

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.

Where does the information about rs151266052 come from?

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.

Quoting this page

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.

Succinic acid/Methylmalonic acid levels (rs151266052). MyGeneLog™. https://www.mygenelog.com/variants/rs151266052

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