SLFN14 · rs17550268
Where this position leads
Condition: Celiac Disease
Strength of the evidence
Its strongest genetic-study result is p = 10−28, with 1 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 394,642 European ancestry individuals.
The effect Each copy of the C allele shifted the measure 0.0245 lower (95% confidence interval 0.02-0.029); p = 4 × 10−29.
How common The C allele had a frequency of about 22% in the people studied.
Where it sits Chromosome 17, band 17q12 — in the 3′ untranslated region of SLFN14.
rs17550268 is a single position in the genome, in or near the SLFN14 gene. Published research associates it with platelet distribution width (ukb data field 30110). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
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.
GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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Platelet distribution width (UKB data field 30110) (rs17550268). MyGeneLog™. https://www.mygenelog.com/variants/rs17550268