Standard

Refractive error

RMI2 · rs1646026

Where this position leads

Condition: Myopia

rs1646026 Condition: Myopia Myopia Condition rs1646026 rs1646026 RMI2

What the study found

Who was studied 144,737 African ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.038 SD unit higher (95% confidence interval 0.025-0.051); p = 3 × 10−8.

How common The T allele had a frequency of about 19% in the people studied.

Where it sits Chromosome 16, band 16p13.13 — inside RMI2.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Refractive error — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Refractive error.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Refractive error compared to the general population.
Source

Questions about rs1646026

What is rs1646026?

rs1646026 is a single position in the genome, in or near the RMI2 gene. Published research associates it with refractive error. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1646026 linked to?

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

Does having rs1646026 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 rs1646026 come from?

GWAS Catalog, Nature genetics 2026, PMID:42009823. 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.

Refractive error (rs1646026). MyGeneLog™. https://www.mygenelog.com/variants/rs1646026

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