ENSG00000232985 · rs1556659
Where this position leads
Condition: Hand Grip Strength
What the study found
Who was studied 334,825 British ancestry individuals.
The effect Each copy of the T allele shifted the measure 0.002 higher (95% confidence interval 0.0014-0.0026); p = 1 × 10−13.
How common The T allele had a frequency of about 38% in the people studied.
Where it sits Chromosome 10, band 10q26.3 — in a non-coding transcript of LOC124902559.
rs1556659 is a single position in the genome, in or near the ENSG00000232985 gene. Published research associates it with hand grip strength. 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 Hand Grip Strength. 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, Sci Rep 2018, PMID:29691431. 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.
Hand grip strength (rs1556659). MyGeneLog™. https://www.mygenelog.com/variants/rs1556659