Standard
Vascular endothelial growth factor levels
MRPL14 · rs4513773
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 with typical/baseline likelihood of Vascular endothelial growth factor levels — no copies of the reported risk allele.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Vascular endothelial growth factor levels.
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Vascular endothelial growth factor levels compared to the general population.
Source
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels
Debette S,
Visvikis-Siest S,
Chen MH,
Ndiaye NC,
Song C,
Destefano A,
Safa R,
Azimi Nezhad M,
Sawyer D,
Marteau JB,
Xanthakis V,
Siest G
and 11 more — show all
Sullivan L,
Pfister M,
Smith H,
Choi SH,
Lamont J,
Lind L,
Yang Q,
Fitzgerald P,
Ingelsson E,
Vasan RS,
Seshadri S
Circulation research · 2011 · PMID 21757650
Questions about rs4513773
What is rs4513773?
rs4513773 is a single position in the genome, in or near the MRPL14 gene. Published research associates it with vascular endothelial growth factor levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4513773 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 rs4513773 come from?
GWAS Catalog, Circ Res 2011, PMID:21757650. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants