A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Height compared to the general population. (GWAS Catalog, Nature 2010, PMID:20881960)
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Height. (GWAS Catalog, Nature 2010, PMID:20881960)
G/GPublished research associates this genotype with typical/baseline likelihood of Height — no copies of the reported risk allele. (GWAS Catalog, Nature 2010, PMID:20881960)
Source: GWAS Catalog, Nature 2010, PMID:20881960
Questions about rs17780086
What is rs17780086?
rs17780086 is a single position in the genome, in or near the LRRC37B gene. Published research associates it with height. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17780086 linked to?
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
Does having rs17780086 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 rs17780086 come from?
GWAS Catalog, Nature 2010, PMID:20881960. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.