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Serum 25-Hydroxyvitamin D levels

CCDST · rs144613541

What the study found

Who was studied 443,734 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0154 higher (95% confidence interval 0.011-0.02); p = 6 × 10−12.

How common The G allele had a frequency of about 29% in the people studied.

Where it sits Chromosome 1, band 1q21.3 — in an intron of CCDST.

What each result means

A/A No copy of the version the research linked to Serum 25-Hydroxyvitamin D levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Serum 25-Hydroxyvitamin D levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Serum 25-Hydroxyvitamin D levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs144613541

What is rs144613541?

rs144613541 is a single position in the genome, in or near the CCDST gene. Published research associates it with serum 25-hydroxyvitamin 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 rs144613541 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 rs144613541 come from?

GWAS Catalog, American journal of human genetics 2020, PMID:32059762. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Serum 25-Hydroxyvitamin D levels (rs144613541). MyGeneLog™. https://www.mygenelog.com/variants/rs144613541

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