Who was studied 426,824 British ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0207 higher (95% confidence interval 0.015-0.027); p = 2 × 10−11.
How common The G allele had a frequency of about 90% in the people studied.
Where it sits Chromosome 14, band 14q22.1 — in an intron of ERO1A.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Heel bone mineral density — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Heel bone mineral density.
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Heel bone mineral density compared to the general population.
Nature genetics · 2019 · PMID 30598549 · open access
Questions about rs3783449
What is rs3783449?
rs3783449 is a single position in the genome, in or near the ERO1A gene. Published research associates it with heel bone mineral density. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3783449 linked to?
On MyGeneLog this position is linked to Heel Bone Mineral Density. The research behind each link, and its sources, are set out on that condition page.
Does having rs3783449 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 rs3783449 come from?
GWAS Catalog, Nat Genet 2018, PMID:30598549. 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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Heel bone mineral density (rs3783449). MyGeneLog™. https://www.mygenelog.com/variants/rs3783449