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Serum 25-Hydroxyvitamin D levels

near SPRR2C · rs184958517

What the study found

Who was studied 443,734 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.135 lower (95% confidence interval 0.1-0.17); p = 6 × 10−15.

How common The T allele had a frequency of about 99% in the people studied.

Where it sits Chromosome 1, band 1q21.3 — between genes, 1.7 kb from SPRR2C.

What each result means

G/G No copy of the version the research linked to Serum 25-Hydroxyvitamin D levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Serum 25-Hydroxyvitamin D levels. That is a smaller link than two copies.
T/T 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 rs184958517

What is rs184958517?

rs184958517 is a single position in the genome, in or near the near SPRR2C 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 rs184958517 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 rs184958517 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 (rs184958517). MyGeneLog™. https://www.mygenelog.com/variants/rs184958517

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