Standard

Vitamin D levels

PDE3B · rs11023332

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 each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Vitamin D levels compared to the general population.

C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Vitamin D levels.

G/G Published research associates this genotype with typical/baseline likelihood of Vitamin D levels — no copies of the reported risk allele.

Source

Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study

Anderson D, Holt BJ, Pennell CE, Holt PG, Hart PH, Blackwell JM

Genes and immunity · 2014 · PMID 25208829

Questions about rs11023332

What is rs11023332?

rs11023332 is a single position in the genome, in or near the PDE3B gene. Published research associates it with vitamin d levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11023332 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 rs11023332 come from?

GWAS Catalog, Genes Immun 2014, PMID:25208829. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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