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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 2,935 Qatari ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.42 lower (95% confidence interval 0.3-0.54); p = 4 × 10−11.
How common The G allele had a frequency of about 4% in the people studied.
Where it sits Chromosome 17, band 17q12 — in an intron of CCL23.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of C-C motif chemokine 16 levels — no copies of the reported risk allele.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with C-C motif chemokine 16 levels.
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of C-C motif chemokine 16 levels compared to the general population.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs117230744
What is rs117230744?
rs117230744 is a single position in the genome, in or near the CCL23 gene. Published research associates it with c-c motif chemokine 16 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117230744 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 rs117230744 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. 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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