Who was studied 21,768 European ancestry individuals, 2,131 Erasmus Rucphen (founder/genetic isolate) individuals; replicated in 8,168 Asian ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.009 lower (95% confidence interval 0.007-0.011); p = 3 × 10−17.
Where it sits Chromosome 20, band 20p12.3 — between genes, 17.9 kb from CASC20.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Vertical cup-disc ratio compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Vertical cup-disc ratio.
G/GPublished research associates this genotype with typical/baseline likelihood of Vertical cup-disc ratio — no copies of the reported risk allele.
rs6107845 is a single position in the genome, in or near the BMP2 gene. Published research associates it with vertical cup-disc ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs6107845 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 rs6107845 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 rs6107845 come from?
GWAS Catalog, Hum Mol Genet 2017, PMID:28073927. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.