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Who was studied 806,834 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0176 lower (95% confidence interval 0.012-0.023); p = 4 × 10−10.
How common The C allele had a frequency of about 91% in the people studied.
Where it sits Chromosome 9, band 9q33.2 — between genes, 45.3 kb from LINC01613.
What each result means
C/CTwo copies of the version the research linked to Body mass index. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/GOne copy of the version the research linked to Body mass index. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Body mass index. This is the starting point the study compared everyone against.
Human molecular genetics · 2019 · PMID 30239722 · open access
Questions about rs10984756
What is rs10984756?
rs10984756 is a single position in the genome, in or near the near LINC01613 gene. Published research associates it with body mass index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs10984756 linked to?
On MyGeneLog this position is linked to Childhood Body Mass Index. The research behind each link, and its sources, are set out on that condition page.
Does having rs10984756 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 rs10984756 come from?
GWAS Catalog, Human molecular genetics 2019, PMID:30239722. 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.
Body mass index (rs10984756). MyGeneLog™. https://www.mygenelog.com/variants/rs10984756