C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Blond vs. brown/black hair color compared to the general population. (GWAS Catalog, Nat Commun 2018, PMID:30531825)
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Blond vs. brown/black hair color. (GWAS Catalog, Nat Commun 2018, PMID:30531825)
T/TPublished research associates this genotype with typical/baseline likelihood of Blond vs. brown/black hair color — no copies of the reported risk allele. (GWAS Catalog, Nat Commun 2018, PMID:30531825)
rs79966207 is a single position in the genome, in or near the PLXNB2 gene. Published research associates it with blond vs. brown/black hair 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 rs79966207 linked to?
On MyGeneLog this position is linked to Hair Color. The research behind each link, and its sources, are set out on that condition page.
Does having rs79966207 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 rs79966207 come from?
GWAS Catalog, Nat Commun 2018, PMID:30531825. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.