Standard
Asymmetrical dimethylarginine levels
DDAH1 · rs2268667
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
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Asymmetrical dimethylarginine levels compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Asymmetrical dimethylarginine levels.
G/G
Published research associates this genotype with typical/baseline likelihood of Asymmetrical dimethylarginine levels — no copies of the reported risk allele.
Source
Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine
Lüneburg N,
Lieb W,
Zeller T,
Chen MH,
Maas R,
Carter AM,
Xanthakis V,
Glazer NL,
Schwedhelm E,
Seshadri S,
Ikram MA,
Longstreth WT Jr
and 32 more — show all
Fornage M,
König IR,
Loley C,
Ojeda FM,
Schillert A,
Wang TJ,
Sticht H,
Kittel A,
König J,
Benjamin EJ,
Sullivan LM,
Bernges I,
Anderssohn M,
Ziegler A,
Gieger C,
Illig T,
Meisinger C,
Wichmann HE,
Wild PS,
Schunkert H,
Psaty BM,
Wiggins KL,
Heckbert SR,
Smith N,
Lackner K,
Lunetta KL,
Blankenberg S,
Erdmann J,
Munzel T,
Grant PJ,
Vasan RS,
Böger RH
Circulation. Cardiovascular genetics · 2014 · PMID 25245031
Questions about rs2268667
What is rs2268667?
rs2268667 is a single position in the genome, in or near the DDAH1 gene. Published research associates it with asymmetrical dimethylarginine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2268667 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 rs2268667 come from?
GWAS Catalog, Circ Cardiovasc Genet 2014, PMID:25245031. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants