RP11-437L7.1a · rs17616633
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 39,011 European ancestry individuals, 2,099 African ancestry individuals, 795 Hispanic individuals, 3,299 Asian ancestry individuals.
The effect Each copy of the T allele shifted the measure 6.02 Zscore lower; p = 7 × 10−11.
Where it sits Chromosome 16, band 16q12.1 — between genes, 135.7 kb from HNRNPA1L3.
rs17616633 is a single position in the genome, in or near the RP11-437L7.1a gene. Published research associates it with white matter hyperintensities. 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 communications 2020, PMID:32358547. 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.
White matter hyperintensities (rs17616633). MyGeneLog™. https://www.mygenelog.com/variants/rs17616633