Standard

Circulating vasoactive peptide levels

F12 · rs2731672

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 Circulating vasoactive peptide levels — 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 Circulating vasoactive peptide levels.

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Circulating vasoactive peptide levels compared to the general population.

Source

Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1

Verweij N, Mahmud H, Mateo Leach I, de Boer RA, Brouwers FP, Yu H, Asselbergs FW, Struck J, Bakker SJ, Gansevoort RT, Munroe PB, Hillege HL

and 4 more — show all

van Veldhuisen DJ, van Gilst WH, Silljé HH, van der Harst P

Hypertension (Dallas, Tex. : 1979) · 2013 · PMID 23381795

What people read about alongside this

Heart and circulation1

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 rs2731672

What is rs2731672?

rs2731672 is a single position in the genome, in or near the F12 gene. Published research associates it with circulating vasoactive peptide 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 rs2731672?

Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs2731672 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 rs2731672 come from?

GWAS Catalog, Hypertension 2013, PMID:23381795. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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