Standard
Insulin-related traits
TCERG1L · rs10829848
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What each result means
C/C
Published research associates this genotype with typical/baseline likelihood of Insulin-related traits — no copies of the reported risk allele.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Insulin-related traits.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Insulin-related traits compared to the general population.
Source
Genome-wide association study identifies novel loci association with fasting insulin and insulin resistance in African Americans
Chen G,
Bentley A,
Adeyemo A,
Shriner D,
Zhou J,
Doumatey A,
Huang H,
Ramos E,
Erdos M,
Gerry N,
Herbert A,
Christman M
and 1 more — show all
Human molecular genetics · 2012 · PMID 22791750
Questions about rs10829848
What is rs10829848?
rs10829848 is a single position in the genome, in or near the TCERG1L gene. Published research associates it with insulin-related traits. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10829848 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 rs10829848 come from?
GWAS Catalog, Hum Mol Genet 2012, PMID:22791750. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants