Standard

Corneal resistance factor (MTAG)

C4orf36 · rs80215053

What the study found

Who was studied 123,734 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0651 lower (95% confidence interval 0.052-0.079); p = 2 × 10−21.

How common The A allele had a frequency of about 91% in the people studied.

Where it sits Chromosome 4, band 4q21.3 — in an intron of C4orf36.

What each result means

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

Questions about rs80215053

What is rs80215053?

rs80215053 is a single position in the genome, in or near the C4orf36 gene. Published research associates it with corneal resistance factor (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs80215053 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 rs80215053 come from?

GWAS Catalog, JAMA ophthalmology 2022, PMID:35446358. 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.

Corneal resistance factor (MTAG) (rs80215053). MyGeneLog™. https://www.mygenelog.com/variants/rs80215053

← See all variants