NFIX · rs76567647
Where this position leads
Condition: Celiac Disease
Strength of the evidence
Its strongest genetic-study result is p = 10−14, 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 T allele shifted the measure 0.0219 lower (95% confidence interval 0.016-0.028); p = 9 × 10−15.
How common The T allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 19, band 19p13.13 — in an intron of NFIX.
rs76567647 is a single position in the genome, in or near the NFIX gene. Published research associates it with platelet crit (ukb data field 30090). 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.
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.
Platelet crit (UKB data field 30090) (rs76567647). MyGeneLog™. https://www.mygenelog.com/variants/rs76567647