C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Self-reported math ability compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Self-reported math ability.
T/TPublished research associates this genotype with typical/baseline likelihood of Self-reported math ability — no copies of the reported risk allele.
rs1850751 is a single position in the genome, in or near the GALNT13 gene. Published research associates it with self-reported math ability. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs1850751 linked to?
On MyGeneLog this position is linked to Educational Attainment. The research behind each link, and its sources, are set out on that condition page.
Does having rs1850751 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 rs1850751 come from?
GWAS Catalog, Nat Genet 2018, PMID:30038396. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.