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Intraocular pressure

ANGPT1 · rs13270051

Where this position leads

Condition: Glaucoma

rs13270051 Condition: Glaucoma Glaucoma Condition rs13270051 rs13270051 ANGPT1

What the study found

Who was studied 115,486 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.227 higher (95% confidence interval 0.19-0.27); p = 9 × 10−31.

How common The C allele had a frequency of about 87% in the people studied.

Where it sits Chromosome 8, band 8q23.1 — in an intron of ANGPT1.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Intraocular pressure compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Intraocular pressure.
T/T Published research associates this genotype with typical/baseline likelihood of Intraocular pressure — no copies of the reported risk allele.
Source
Genome-wide association analyses identify new loci influencing intraocular pressure
Gao XR, Huang H, Nannini DR, Fan F, Kim H
Human molecular genetics · 2018 · PMID 29617998

Questions about rs13270051

What is rs13270051?

rs13270051 is a single position in the genome, in or near the ANGPT1 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 rs13270051 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 rs13270051 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 rs13270051 come from?

GWAS Catalog, Hum Mol Genet 2018, PMID:29617998. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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