Standard

Glaucoma

SRBD1 · rs3213787

Where this position leads

Condition: Glaucoma

rs3213787 Condition: Glaucoma Glaucoma Condition rs3213787 rs3213787 SRBD1

What the study found

Who was studied 305 Japanese ancestry cases, 355 Japanese ancestry controls.

The effect Each copy of the A allele carried 2.80 times the odds of Glaucoma (95% confidence interval 1.96-3.99); p = 3 × 10−9.

How common The A allele had a frequency of about 81% in the people studied.

Where it sits Chromosome 2, band 2p21 — in an intron of SRBD1.

What each result means

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

Questions about rs3213787

What is rs3213787?

rs3213787 is a single position in the genome, in or near the SRBD1 gene. Published research associates it with glaucoma. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3213787 linked to?

On MyGeneLog this position is linked to Glaucoma. The research behind each link, and its sources, are set out on that condition page.

Does having rs3213787 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 rs3213787 come from?

GWAS Catalog, Ophthalmology 2010, PMID:20363506. 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.

Glaucoma (rs3213787). MyGeneLog™. https://www.mygenelog.com/variants/rs3213787

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