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Retinal arteriolar tortuosity

KLHL2P1 · rs11727963

What the study found

Who was studied 52,798 European ancestry individuals; replicated in 4,987 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.06 lower (95% confidence interval 0.052-0.068); p = 7 × 10−58.

How common The G allele had a frequency of about 83% in the people studied.

Where it sits Chromosome 4, band 4q26 — in an intron of KLHL2P1.

What each result means

A/A No copy of the version the research linked to Retinal arteriolar tortuosity. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Retinal arteriolar tortuosity. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Retinal arteriolar tortuosity. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs11727963

What is rs11727963?

rs11727963 is a single position in the genome, in or near the KLHL2P1 gene. Published research associates it with retinal arteriolar tortuosity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11727963 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 rs11727963 come from?

GWAS Catalog, PLoS genetics 2023, PMID:36757925. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Retinal arteriolar tortuosity (rs11727963). MyGeneLog™. https://www.mygenelog.com/variants/rs11727963

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