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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 30,708 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 8.51 z score higher; p = 2 × 10−17.
Where it sits Chromosome 3, band 3q27.1 — in an intron of KLHL24.
What each result means
A/ANo copy of the version the research linked to White matter hyperintensities. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to White matter hyperintensities. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to White matter hyperintensities. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2024 · PMID 38890310 · open access
Questions about rs830179
What is rs830179?
rs830179 is a single position in the genome, in or near the KLHL24 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.
Does having rs830179 mean I will get this?
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.
Where does the information about rs830179 come from?
GWAS Catalog, Nature communications 2024, PMID:38890310. 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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Quoting this page
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 (rs830179). MyGeneLog™. https://www.mygenelog.com/variants/rs830179