Standard

Eye color

TYR · rs1393350

Where this position leads

Condition: Eye Color and Pigmentation

rs1393350 Condition: Eye Color and Pigmentation Eye Color and Pigmentation Condition rs1393350 rs1393350 TYR

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Eye color compared to the general population. (GWAS Catalog, PLoS Genet 2010, PMID:20585627)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Eye color. (GWAS Catalog, PLoS Genet 2010, PMID:20585627)
G/G Published research associates this genotype with typical/baseline likelihood of Eye color — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2010, PMID:20585627)

Source: GWAS Catalog, PLoS Genet 2010, PMID:20585627

What people read about alongside this

Skin, sun and hair1

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs1393350

What is rs1393350?

rs1393350 is a single position in the genome, in or near the TYR gene. Published research associates it with eye color. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs1393350 linked to?

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

What do people read about alongside rs1393350?

Subjects that appear in the title or abstract of the same papers as this rsID include skin, sun and hair (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs1393350 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 rs1393350 come from?

GWAS Catalog, PLoS Genet 2010, PMID:20585627. 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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