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Who was studied 290 African American or Afro-Caribbean cases, 121,440 African American or Afro-Caribbean controls, 430 European ancestry cases, 450,463 European ancestry controls.
The effect
Each copy of the C allele shifted the measure 2.52 lower (95% confidence interval 2.48-2.56); p = 3 × 10−11.
How common The C allele had a frequency of about 100% in the people studied.
Where it sits Chromosome 6, band 6q25.1 — in an intron of LRP11.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Unspecified diffuse connective tissue disease (PheCode 709.7) compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Unspecified diffuse connective tissue disease (PheCode 709.7).
T/TPublished research associates this genotype with typical/baseline likelihood of Unspecified diffuse connective tissue disease (PheCode 709.7) — no copies of the reported risk allele.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs570063769
What is rs570063769?
rs570063769 is a single position in the genome, in or near the LRP11 gene. Published research associates it with unspecified diffuse connective tissue disease (phecode 709.7). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs570063769 linked to?
On MyGeneLog this position is linked to Unspecified Diffuse Connective Tissue Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs570063769 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 rs570063769 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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