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Serum 25-Hydroxyvitamin D levels

PHACTR3 · rs1014490316

What the study found

Who was studied 5,885 Qatari ancestry individuals; replicated in 7,767 Qatari ancestry individuals.

The effect Each copy of the G allele shifted the measure 2.65 higher; p = 5 × 10−8.

How common The G allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 20, band 20q13.32 — in an intron of PHACTR3.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Serum 25-Hydroxyvitamin D levels — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum 25-Hydroxyvitamin D levels.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum 25-Hydroxyvitamin D levels compared to the general population.
Source

Questions about rs1014490316

What is rs1014490316?

rs1014490316 is a single position in the genome, in or near the PHACTR3 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 rs1014490316 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 rs1014490316 come from?

GWAS Catalog, International journal of molecular sciences 2025, PMID:41096749. 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 (rs1014490316). MyGeneLog™. https://www.mygenelog.com/variants/rs1014490316

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