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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 47,740 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0398 lower (95% confidence interval 0.028-0.052); p = 2 × 10−10.
Where it sits Chromosome 11, band 11p11.2 — in an intron of ALX4.
What each result means
A/ATwo copies of the version the research linked to Cardiac MRI latent phenotype (Z26_S3). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Cardiac MRI latent phenotype (Z26_S3). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Cardiac MRI latent phenotype (Z26_S3). This is the starting point the study compared everyone against.
Nature communications · 2026 · PMID 42373625 · open access
Questions about rs4755800
What is rs4755800?
rs4755800 is a single position in the genome, in or near the ALX4 gene. Published research associates it with cardiac mri latent phenotype (z26_s3). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4755800 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 rs4755800 come from?
GWAS Catalog, Nature communications 2026, PMID:42373625. 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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