Standard
Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype)
RAB11FIP5 · rs58649746
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
A/A
Published research associates this genotype with typical/baseline likelihood of Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) — 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 Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype).
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) compared to the general population.
Source
Multidimensional Bone Density Phenotyping Reveals New Insights Into Genetic Regulation of the Pediatric Skeleton
Mitchell JA,
Chesi A,
Cousminer DL,
McCormack SE,
Kalkwarf HJ,
Lappe JM,
Gilsanz V,
Oberfield SE,
Shepherd JA,
Kelly A,
Zemel BS,
Grant SF
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2018 · PMID 29240982
Questions about rs58649746
What is rs58649746?
rs58649746 is a single position in the genome, in or near the RAB11FIP5 gene. Published research associates it with pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs58649746 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 rs58649746 come from?
GWAS Catalog, J Bone Miner Res 2017, PMID:29240982. 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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