PER3 Gene
Period Circadian Regulator 3 (PER3) is a gene involved in circadian clock that has been studied in relation to immune function, metabolism, and chronic illness. Variants in PER3 may influence how the body responds to infection, inflammation, and long-term recovery.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the PER3 gene?
PER3 encodes period circadian regulator 3, a protein involved in circadian clock. It belongs to the Circadian Rhythm category and is part of the Neurological & Sleep biological cluster. PER3 encodes a circadian clock component with a variable number tandem repeat (VNTR) polymorphism affecting sleep phenotypes. The 5-repeat allele is associated with morning preference while the 4-repeat allele associates with delayed sleep phase.
Biological role and pathway
PER3 is involved in the circadian clock pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Neurological & Sleep cluster work together to maintain balanced function across interconnected biological systems.
Variants in genes within this pathway may influence an individual's predisposition to altered function in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.
PER3 and Long COVID / ME-CFS research
The PER3 VNTR polymorphism influences sleep duration, sleep homeostasis, and cognitive performance following sleep deprivation — all relevant to the sleep dysfunction and cognitive impairment characterizing Long COVID brain fog.
This information is based on published research and does not constitute medical advice. See references below.
Known genetic variants
The following variants (SNPs) in the PER3 gene have been studied in relation to circadian rhythm and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs57875989— PER3 variant
- rs228697— PER3 variant
- rs10462021— PER3 variant
Conditions studied in relation to PER3
Research into PER3 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that PER3 causes or treats any condition.
Genetic insights from DNA data
Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include PER3 and related genes in the neurological & sleep pathway.
The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.
Related genes in the Neurological & Sleep pathway
PER3 does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.
Frequently asked questions
What is the PER3 gene and what does it do?
PER3 (Period Circadian Regulator 3) is involved in circadian clock. PER3 encodes a circadian clock component with a variable number tandem repeat (VNTR) polymorphism affecting sleep phenotypes. The 5-repeat allele is associated with morning preference while the 4-repeat allele associates with delayed sleep phase.
How may PER3 gene variants relate to Long COVID or ME/CFS?
The PER3 VNTR polymorphism influences sleep duration, sleep homeostasis, and cognitive performance following sleep deprivation — all relevant to the sleep dysfunction and cognitive impairment characterizing Long COVID brain fog.
Can a DNA test reveal information about my PER3 gene?
Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Explore your PER3 genetic insights
Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.
Get Your Personalised DNA ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for PER3. This is not an exhaustive literature review.
- [1]PMID: 12939611
- [2]Current Biology
- [3]Sleep