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Platelet-derived growth factor D levels

PDGFD · rs7115797

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.457 lower (95% confidence interval 0.43-0.48); p = 1 × 10−242.

How common The A allele had a frequency of about 29% in the people studied.

Where it sits Chromosome 11, band 11q22.3 — in an intron of PDGFD.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Platelet-derived growth factor D 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 Platelet-derived growth factor D levels.
G/G Published research associates this genotype with typical/baseline likelihood of Platelet-derived growth factor D levels — no copies of the reported risk allele.
Source

Questions about rs7115797

What is rs7115797?

rs7115797 is a single position in the genome, in or near the PDGFD gene. Published research associates it with platelet-derived growth factor d levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7115797 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 rs7115797 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Platelet-derived growth factor D levels (rs7115797). MyGeneLog™. https://www.mygenelog.com/variants/rs7115797

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