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Vascular endothelial growth factor levels

CAPN11 · rs7763358

What each result means

C/C 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.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Vascular endothelial growth factor levels.
T/T Published research associates this genotype with typical/baseline likelihood of Vascular endothelial growth factor levels — no copies of the reported risk allele.
Source

Questions about rs7763358

What is rs7763358?

rs7763358 is a single position in the genome, in or near the CAPN11 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 rs7763358 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 rs7763358 come from?

GWAS Catalog, Am J Hum Genet 2016, PMID:27989323. 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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