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Who was studied up to 248,507 non-Hispanic white individuals, up to 68,155 non-Hispanic black individuals, up to 25,847 Hispanic individuals, up to 3,054 Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.06 higher; p = 2 × 10−10.
Where it sits Chromosome 1, band 1p31.1 — in an intron of ZRANB2-DT.
What each result means
A/ANo copy of the version the research linked to Height. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Height. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Height. That is the strongest link of the three results. A link in a study is not a diagnosis.
American journal of human genetics · 2019 · PMID 31564439
Questions about rs17097556
What is rs17097556?
rs17097556 is a single position in the genome, in or near the ZRANB2-DT gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17097556 linked to?
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
Does having rs17097556 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 rs17097556 come from?
GWAS Catalog, American journal of human genetics 2019, PMID:31564439. 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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