A/APublished 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/CPublished 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)
C/CPublished 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)
rs1847134 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 rs1847134 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.
Does having rs1847134 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 rs1847134 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.