Standard
Pediatric bone mineral content (radius)
CPED1 · rs34770628
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
C/C
Published research associates this genotype with typical/baseline likelihood of Pediatric bone mineral content (radius) — no copies of the reported risk allele.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pediatric bone mineral content (radius).
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Pediatric bone mineral content (radius) compared to the general population.
Source
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites
Chesi A,
Mitchell JA,
Kalkwarf HJ,
Bradfield JP,
Lappe JM,
Cousminer DL,
Roy SM,
McCormack SE,
Gilsanz V,
Oberfield SE,
Hakonarson H,
Shepherd JA
and 3 more — show all
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017 · PMID 28181694
Questions about rs34770628
What is rs34770628?
rs34770628 is a single position in the genome, in or near the CPED1 gene. Published research associates it with pediatric bone mineral content (radius). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs34770628 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 rs34770628 come from?
GWAS Catalog, J Bone Miner Res 2017, PMID:28181694. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants