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Optic cup area

RERE · rs301801

What the study found

Who was studied 15,087 European ancestry individuals, 2,131 Erasmus Rucphen Family individuals; replicated in 2,363 Chinese ancestry individuals, 2,225 Malay ancestry individuals, 2,025 Indian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.016 higher (95% confidence interval 0.010-0.022); p = 5 × 10−9.

How common The C allele had a frequency of about 33% in the people studied.

Where it sits Chromosome 1, band 1p36.23 — in an intron of RERE.

What each result means

C/C Two copies of the version the research linked to Optic cup area. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Optic cup area. That is a smaller link than two copies.
T/T No copy of the version the research linked to Optic cup area. This is the starting point the study compared everyone against.
Source

Questions about rs301801

What is rs301801?

rs301801 is a single position in the genome, in or near the RERE gene. Published research associates it with optic cup area. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs301801 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 rs301801 come from?

GWAS Catalog, Genetic epidemiology 2015, PMID:25631615. 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.

Optic cup area (rs301801). MyGeneLog™. https://www.mygenelog.com/variants/rs301801

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