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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 5,348 Icelandic ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.157 lower (95% confidence interval 0.12-0.19); p = 9 × 10−16.
How common The G allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 22, band 22q13.31 — between genes, 6.6 kb from MIRLET7BHG.
What each result means
C/CNo copy of the version the research linked to Serum levels of protein CCL27. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Serum levels of protein CCL27. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Serum levels of protein CCL27. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2022 · PMID 35078996 · open access
Questions about rs9616196
What is rs9616196?
rs9616196 is a single position in the genome, in or near the near MIRLET7BHG gene. Published research associates it with serum levels of protein ccl27. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9616196 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 rs9616196 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 CCL27 (rs9616196). MyGeneLog™. https://www.mygenelog.com/variants/rs9616196