C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Fasting blood glucose compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Fasting blood glucose.
T/TPublished research associates this genotype with typical/baseline likelihood of Fasting blood glucose — no copies of the reported risk allele.
PLoS genetics · 2018 · PMID 29621232 · open access
Questions about rs13387347
What is rs13387347?
rs13387347 is a single position in the genome, in or near the SPC25 gene. Published research associates it with fasting blood glucose. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs13387347 linked to?
On MyGeneLog this position is linked to Fasting Blood Glucose. The research behind each link, and its sources, are set out on that condition page.
Does having rs13387347 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 rs13387347 come from?
GWAS Catalog, PLoS Genet 2018, PMID:29621232. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.