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Height

ISM1 · rs729646

Where this position leads

Condition: Height

rs729646 Condition: Height Height Condition rs729646 rs729646 ISM1

What the study found

Who was studied 455,180 Hispanic or Latin American individuals.

The effect Each copy of the A allele shifted the measure 0.0169 higher (95% confidence interval 0.012-0.022); p = 2 × 10−10.

How common The A allele had a frequency of about 20% in the people studied.

Where it sits Chromosome 20, band 20p12.1 — in an intron of ISM1.

What each result means

A/A Two 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.
A/C One copy of the version the research linked to Height. That is a smaller link than two copies.
C/C No copy of the version the research linked to Height. This is the starting point the study compared everyone against.
Source

Questions about rs729646

What is rs729646?

rs729646 is a single position in the genome, in or near the ISM1 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 rs729646 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 rs729646 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 rs729646 come from?

GWAS Catalog, Nature 2022, PMID:36224396. 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 (rs729646). MyGeneLog™. https://www.mygenelog.com/variants/rs729646

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