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Trans-laminar cribrosa pressure difference

MAMDC2 · rs75529319

What the study found

Who was studied 82,147 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.114 higher (95% confidence interval 0.075-0.153); p = 1 × 10−8.

How common The T allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 9, band 9q21.12 — in an intron of MAMDC2.

What each result means

C/C No copy of the version the research linked to Trans-laminar cribrosa pressure difference. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Trans-laminar cribrosa pressure difference. That is a smaller link than two copies.
T/T 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 rs75529319

What is rs75529319?

rs75529319 is a single position in the genome, in or near the MAMDC2 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 rs75529319 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 rs75529319 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

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Trans-laminar cribrosa pressure difference (rs75529319). MyGeneLog™. https://www.mygenelog.com/variants/rs75529319

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