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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 12,586 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.242 higher (95% confidence interval 0.17-0.31); p = 1 × 10−10.
How common The A allele had a frequency of about 60% in the people studied.
Where it sits Chromosome 2, band 2q31.1 — between genes, 1.4 kb from HOXD13.
What each result means
A/ATwo copies of the version the research linked to Digit length ratio. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Digit length ratio. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Digit length ratio. This is the starting point the study compared everyone against.
Human molecular genetics · 2018 · PMID 29659830 · open access
Questions about rs847158
What is rs847158?
rs847158 is a single position in the genome, in or near the HOXD12 gene. Published research associates it with digit length ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs847158 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 rs847158 come from?
GWAS Catalog, Hum Mol Genet 2018, PMID:29659830. 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.
Digit length ratio (rs847158). MyGeneLog™. https://www.mygenelog.com/variants/rs847158