near SLC39A8 · rs61161339
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.
Strength of the evidence
Its strongest genetic-study result is p = 10−9, 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 35,474 European ancestry individuals.
The effect Each copy of the G allele shifted the measure 0.0576 lower (95% confidence interval 0.039-0.076); p = 1 × 10−9.
How common The G allele had a frequency of about 17% in the people studied.
Where it sits Chromosome 4, band 4q24 — between genes, 79.7 kb from SLC39A8.
rs61161339 is a single position in the genome, in or near the near SLC39A8 gene. Published research associates it with volume of left central nucleus. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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:40097784. 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.
Volume of left central nucleus (rs61161339). MyGeneLog™. https://www.mygenelog.com/variants/rs61161339