Standard

Height (baseline)

near LYNX1-SLURP2 · rs373472791

Where this position leads

Condition: Height

rs373472791 Condition: Height Height Condition rs373472791 rs373472791 near LYNX1-S…

What the study found

Who was studied 405,540 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.00854 higher (95% confidence interval 0.0056-0.0114); p = 7 × 10−9.

How common The C allele had a frequency of about 66% in the people studied.

Where it sits Chromosome 8, band 8q24.3 — between genes, 4.2 kb from LYNX1-SLURP2.

What each result means

C/C Two copies of the version the research linked to Height (baseline). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Height (baseline). That is a smaller link than two copies.
T/T No copy of the version the research linked to Height (baseline). This is the starting point the study compared everyone against.
Source

Questions about rs373472791

What is rs373472791?

rs373472791 is a single position in the genome, in or near the near LYNX1-SLURP2 gene. Published research associates it with height (baseline). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs373472791 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 rs373472791 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 rs373472791 come from?

GWAS Catalog, Nature communications 2025, PMID:40374629. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Height (baseline) (rs373472791). MyGeneLog™. https://www.mygenelog.com/variants/rs373472791

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