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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 342,535 European ancestry individuals, 6,019 African ancestry individuals, 7,337 South Asian ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0252 higher (95% confidence interval 0.018-0.033); p = 4 × 10−11.
Where it sits Chromosome 6, band 6p22.3 — in an intron of KIAA0319.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum alkaline phosphatase levels compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum alkaline phosphatase levels.
T/TPublished research associates this genotype with typical/baseline likelihood of Serum alkaline phosphatase levels — no copies of the reported risk allele.
Nature genetics · 2021 · PMID 33462484 · open access
Questions about rs17307478
What is rs17307478?
rs17307478 is a single position in the genome, in or near the KIAA0319 gene. Published research associates it with serum alkaline phosphatase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17307478 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 rs17307478 come from?
GWAS Catalog, Nature genetics 2021, PMID:33462484. 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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