Standard

Metabolite levels

ETFDH · rs8396

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Metabolite levels — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2009, PMID:20037589)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Metabolite levels. (GWAS Catalog, Nat Genet 2009, PMID:20037589)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Metabolite levels compared to the general population. (GWAS Catalog, Nat Genet 2009, PMID:20037589)

Source: GWAS Catalog, Nat Genet 2009, PMID:20037589

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs8396

What is rs8396?

rs8396 is a single position in the genome, in or near the ETFDH gene. Published research associates it with metabolite levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What do people read about alongside rs8396?

Subjects that appear in the title or abstract of the same papers as this rsID include exercise and muscle (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs8396 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 rs8396 come from?

GWAS Catalog, Nat Genet 2009, PMID:20037589. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

← See all variants