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Erlin-1 levels

HTRA1 · rs2300431

What the study found

Who was studied 3,506 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.218 higher (95% confidence interval 0.17-0.27); p = 9 × 10−16.

How common The A allele had a frequency of about 26% in the people studied.

Where it sits Chromosome 10, band 10q26.13 — in an intron of HTRA1.

What each result means

A/A Two copies of the version the research linked to Erlin-1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Erlin-1 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Erlin-1 levels. This is the starting point the study compared everyone against.
Source

Questions about rs2300431

What is rs2300431?

rs2300431 is a single position in the genome, in or near the HTRA1 gene. Published research associates it with erlin-1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2300431 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 rs2300431 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. 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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Erlin-1 levels (rs2300431). MyGeneLog™. https://www.mygenelog.com/variants/rs2300431

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