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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 5,367 Icelandic ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.463 lower (95% confidence interval 0.33-0.6); p = 4 × 10−11.
How common The C allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 2, band 2p13.3 — in an intron of ANTXR1.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Serum levels of protein GKN2 — no copies of the reported risk allele.
A/CPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum levels of protein GKN2.
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum levels of protein GKN2 compared to the general population.
Nature communications · 2022 · PMID 35078996 · open access
Questions about rs11693609
What is rs11693609?
rs11693609 is a single position in the genome, in or near the ANTXR1 gene. Published research associates it with serum levels of protein gkn2. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11693609 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 rs11693609 come from?
GWAS Catalog, Nature communications 2022, PMID:35078996. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Serum levels of protein GKN2 (rs11693609). MyGeneLog™. https://www.mygenelog.com/variants/rs11693609