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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 2,294 White British ancestry female individuals.
The effect
Each copy of the G allele shifted the measure 108 g higher; p = 4 × 10−8.
Where it sits Chromosome 14, band 14q12 — in an intron of NOVA1-DT.
What each result means
G/GTwo copies of the version the research linked to Trunk bone mineral content. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Trunk bone mineral content. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Trunk bone mineral content. This is the starting point the study compared everyone against.
Frontiers in endocrinology · 2021 · PMID 34239500 · open access
Questions about rs112098641
What is rs112098641?
rs112098641 is a single position in the genome, in or near the NOVA1-DT gene. Published research associates it with trunk bone mineral content. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs112098641 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 rs112098641 come from?
GWAS Catalog, Frontiers in endocrinology 2021, PMID:34239500. 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.
Trunk bone mineral content (rs112098641). MyGeneLog™. https://www.mygenelog.com/variants/rs112098641