ELAPOR2 · rs77149046
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 the study found
Who was studied 75 cases from twins, 1,036 controls from twins.
The effect Each copy of the C allele carried 5.40 times the odds of Revision surgery due to aseptic loosening after total joint arthroplasty (95% confidence interval 3.23-9.02); p = 1 × 10−10.
How common The C allele had a frequency of about 4% in the people studied.
Where it sits Chromosome 7, band 7q21.12 — in an intron of ELAPOR2.
rs77149046 is a single position in the genome, in or near the ELAPOR2 gene. Published research associates it with revision surgery due to aseptic loosening after total joint arthroplasty. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
GWAS Catalog, The Journal of bone and joint surgery. American volume 2022, PMID:34982741. 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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Revision surgery due to aseptic loosening after total joint arthroplasty (rs77149046). MyGeneLog™. https://www.mygenelog.com/variants/rs77149046