rs1005473
Variant in the CSNK1E gene (Casein Kinase 1 Epsilon)
rs1005473 is a single nucleotide polymorphism (SNP) in the CSNK1E gene, involved in circadian clock period regulation. Variants at this position have been studied in relation to immune function, metabolism, and chronic illness.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the rs1005473 variant?
rs1005473 is a SNP (single nucleotide polymorphism) in the CSNK1E (Casein Kinase 1 Epsilon) gene. It belongs to the Circadian category and is part of the Sleep & Circadian Rhythm biological cluster. CSNK1E encodes casein kinase 1 epsilon, which phosphorylates PER proteins to regulate their nuclear entry and circadian period.
Biological role and pathway
This variant sits within the CSNK1E gene, which is involved in the circadian clock period regulation pathway. Genes within the Sleep & Circadian Rhythm 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 — particularly under conditions of physiological stress such as viral infection or prolonged illness.
rs1005473 and Long COVID / ME-CFS research
CSNK1E variants affecting PER phosphorylation may alter circadian period length and sleep timing relevant to Long COVID sleep disturbances.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: CSNK1E
rs1005473 is one of 1 known variant in the CSNK1E gene. To understand the full biological context of this variant, explore the parent gene page.
View CSNK1E gene page →Conditions studied in relation to rs1005473
Research into CSNK1E variants including rs1005473 has explored associations with the following conditions. These are areas of scientific investigation and do not imply causation.
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 CSNK1E and the rs1005473 variant.
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.
Frequently asked questions
What is the rs1005473 variant in the CSNK1E gene?
rs1005473 is a single nucleotide polymorphism (SNP) located in the CSNK1E (Casein Kinase 1 Epsilon) gene, which is involved in circadian clock period regulation. CSNK1E encodes casein kinase 1 epsilon, which phosphorylates PER proteins to regulate their nuclear entry and circadian period.
How may the rs1005473 variant relate to Long COVID or ME/CFS?
CSNK1E variants affecting PER phosphorylation may alter circadian period length and sleep timing relevant to Long COVID sleep disturbances.
Can a consumer DNA test detect the rs1005473 variant?
Many consumer DNA tests such as 23andMe, AncestryDNA, and MyHeritage genotype common SNPs. ChronicDNA analyses your raw DNA file and reports on variants studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Find out if you carry the rs1005473 variant
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 CSNK1E and its variants. This is not an exhaustive literature review.
- [1]PMID: 32127339
- [2]Nature Genetics
- [3]Journal of Clinical Investigation