Standard

Intraocular pressure

LINC00970 · rs3007364

Where this position leads

Condition: Intraocular Pressure

rs3007364 Condition: Intraocular Pressure Intraocular Pressure Condition rs3007364 rs3007364 LINC00970

What the study found

Who was studied 101,939 European ancestry cases.

The effect Each copy of the G allele shifted the measure 0.11 higher (95% confidence interval 0.071-0.149); p = 3 × 10−11.

Where it sits Chromosome 1, band 1q24.2 — in an intron of LINC00970.

What each result means

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

Questions about rs3007364

What is rs3007364?

rs3007364 is a single position in the genome, in or near the LINC00970 gene. Published research associates it with intraocular pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3007364 linked to?

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

Does having rs3007364 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 rs3007364 come from?

GWAS Catalog, JAMA ophthalmology 2020, PMID:32352494. 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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Intraocular pressure (rs3007364). MyGeneLog™. https://www.mygenelog.com/variants/rs3007364

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