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Trans-laminar cribrosa pressure difference

near RPL13AP13 · rs1423422

What the study found

Who was studied 82,147 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0319 lower (95% confidence interval 0.023-0.041); p = 1 × 10−11.

How common The G allele had a frequency of about 44% in the people studied.

Where it sits Chromosome 5, band 5q11.2 — between genes, 128.5 kb from RPL13AP13.

What each result means

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

Questions about rs1423422

What is rs1423422?

rs1423422 is a single position in the genome, in or near the near RPL13AP13 gene. Published research associates it with trans-laminar cribrosa pressure difference. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1423422 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 rs1423422 come from?

GWAS Catalog, Investigative ophthalmology & visual science 2026, PMID:42017308. 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.

Trans-laminar cribrosa pressure difference (rs1423422). MyGeneLog™. https://www.mygenelog.com/variants/rs1423422

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